A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974606



Internal ID18609817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:78704441..78755995hg38UCSC Ensembl
Innerchr15:78996783..79048337hg19UCSC Ensembl
Innerchr15:76783838..76835392hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3851555
hg1951555
hg1851555
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2031981, nssv2031978, nssv2031980, nssv2031985, nssv2031976, nssv2031977, nssv2031982, nssv2031983, nssv2031979, nssv2031984
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC646938
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974606
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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