A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036124



Internal ID19125343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:39160951..39263429hg38UCSC Ensembl
Innerchr13:39735088..39837566hg19UCSC Ensembl
Innerchr13:38633088..38735566hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38102479
hg19102479
hg18102479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1632n100
Supporting Variantsnssv3523384
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)nsv1036124
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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