A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977689



Internal ID18266209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30384120..30435489hg38UCSC Ensembl
Innerchr15:30676323..30727692hg19UCSC Ensembl
Innerchr15:28463615..28514984hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3851370
hg1951370
hg1851370
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2014665, nssv2014670, nssv2014669, nssv2014667, nssv2014674, nssv2014673, nssv2014666, nssv2014671, nssv2014672, nssv2014668
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesCHRFAM7A, LOC101059918
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977689
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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