A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974610



Internal ID18609821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:79941862..79947558hg38UCSC Ensembl
Innerchr15:80234204..80239900hg19UCSC Ensembl
Innerchr15:78021259..78026955hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg385697
hg195697
hg185697
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2034158, nssv2034149, nssv2034153, nssv2034152, nssv2034156, nssv2034150, nssv2034157, nssv2034154, nssv2034155, nssv2034151
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974610
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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