A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977736



Internal ID18266256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75216954..75340338hg38UCSC Ensembl
Innerchr15:75509295..75632679hg19UCSC Ensembl
Innerchr15:73296348..73419732hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38123385
hg19123385
hg18123385
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2030401, nssv2030395, nssv2030397, nssv2030400, nssv2030396, nssv2030398, nssv2030403, nssv2030394, nssv2030399, nssv2030402
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesCOMMD4, GOLGA6C, GOLGA6D
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977736
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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