A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067142



Internal ID19156361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45721722..45749572hg38UCSC Ensembl
Innerchr20:44350361..44378211hg19UCSC Ensembl
Innerchr20:43783775..43811618hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3827851
hg1927851
hg1827844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4321n100
Supporting Variantsnssv3584921, nssv3584922, nssv3731350, nssv3584917, nssv3584913, nssv3584907, nssv3584912, nssv3584915, nssv3731351, nssv3584924, nssv3731354, nssv3584908, nssv3584910, nssv3731356, nssv3731347, nssv3584904, nssv3584902, nssv3584906, nssv3584900, nssv3584914, nssv3584899, nssv3584909, nssv3731355, nssv3731346, nssv3731349, nssv3584920, nssv3731353, nssv3584923, nssv3731352, nssv3584919, nssv3584916, nssv3584901, nssv3731348, nssv3731343, nssv3731341, nssv3731345, nssv3584925, nssv3584898, nssv3731340, nssv3584903, nssv3584918, nssv3731357, nssv3731342, nssv3584911, nssv3731344, nssv3584905
Samples
Known GenesSPINT4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067142
Frequency
Sample Size11257
Observed Gain0
Observed Loss46
Observed Complex0
Frequencyn/a


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