A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059752



Internal ID19148971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59849686..59924573hg38UCSC Ensembl
Innerchr20:58424741..58499628hg19UCSC Ensembl
Innerchr20:57858136..57933023hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3874888
hg1974888
hg1874888
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4335n100
Supporting Variantsnssv3584264, nssv3584265
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)nsv1059752
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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