A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035381



Internal ID19124600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55575752..55679201hg38UCSC Ensembl
Innerchr13:56149887..56253335hg19UCSC Ensembl
Innerchr13:55047888..55151336hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38103450
hg19103449
hg18103449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1658n100
Supporting Variantsnssv3714991
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)nsv1035381
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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