A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977383



Internal ID18612589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:41733924..41736660hg38UCSC Ensembl
Innerchr13:42308060..42310796hg19UCSC Ensembl
Innerchr13:41206060..41208796hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg382737
hg192737
hg182737
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2760455, nssv2764984
SamplesHGDP00998, HGDP00778
Known GenesVWA8
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977383
Frequency
Sample Size10
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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