A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038176



Internal ID18780707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70898018..71772254hg38UCSC Ensembl
Innerchr13:71472150..72346386hg19UCSC Ensembl
Innerchr13:70370151..71244387hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38874237
hg19874237
hg18874237
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530497
Samples
Known GenesDACH1, LINC00348
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038176
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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