A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063750



Internal ID18806281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59847994..59922116hg38UCSC Ensembl
Innerchr20:58423049..58497171hg19UCSC Ensembl
Innerchr20:57856444..57930566hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3874123
hg1974123
hg1874123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4335n100
Supporting Variantsnssv3584260, nssv3584261
Samples
Known GenesSYCP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063750
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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