A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969671



Internal ID18604898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64407350..64409983hg38UCSC Ensembl
Innerchr9:69419768..69422401hg19UCSC Ensembl
Innerchr9:68709588..68712221hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg382634
hg192634
hg182634
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2742866, nssv2745790, nssv2742867, nssv2742859, nssv2745795, nssv2745786, nssv2742858, nssv2745794, nssv2742863, nssv2745793, nssv2745788, nssv2742862, nssv2745791, nssv2742864, nssv2745789, nssv2742861, nssv2745787, nssv2742865, nssv2742860, nssv2745792
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A4
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969671
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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