A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972737



Internal ID18607953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62884949..62931304hg38UCSC Ensembl
Innerchr9:66540773..66587128hg19UCSC Ensembl
Innerchr9:66280593..66326948hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3846356
hg1946356
hg1846356
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2738392, nssv2738395, nssv2738401, nssv2738397, nssv2738394, nssv2738400, nssv2738399, nssv2738396, nssv2738398, nssv2738393
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMGC21881
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972737
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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