A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973695



Internal ID18608910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67849063..67859419hg38UCSC Ensembl
Innerchr9:67916302..67926865hg19UCSC Ensembl
Innerchr9:67506122..67516685hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3810357
hg1910564
hg1810564
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2739021, nssv2739025, nssv2739027, nssv2739087, nssv2739079, nssv2739886, nssv2739891, nssv2739091, nssv2739086, nssv2739885, nssv2739889, nssv2739892, nssv2739084, nssv2739029, nssv2739884, nssv2739028, nssv2739887, nssv2739083, nssv2739081, nssv2739022, nssv2739890, nssv2739088, nssv2739026, nssv2739030, nssv2739888, nssv2739024, nssv2739023, nssv2739085, nssv2739080, nssv2739082
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A1, ANKRD20A3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973695
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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