A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2761299



Internal ID17528268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:78653482..78704441hg38UCSC Ensembl
Innerchr15:78945824..78996783hg19UCSC Ensembl
Innerchr15:76732879..76783838hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3850960
hg1950960
hg1850960
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv974713
Supporting Variants
SamplesHGDP01284
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2761299
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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