A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012339



Internal ID19101557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:59131065..59156377hg38UCSC Ensembl
Innerchr4:59996783..60022095hg19UCSC Ensembl
Innerchr4:59679378..59704690hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3825313
hg1925313
hg1825313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3626506
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012339
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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