A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964630



Internal ID18599867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38960507..38992130hg38UCSC Ensembl
Innerchr22:39356512..39388135hg19UCSC Ensembl
Innerchr22:37686458..37718081hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3831624
hg1931624
hg1831624
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2757608, nssv2759827, nssv2766535, nssv2762519, nssv2763529, nssv2766217, nssv2764918, nssv2758121, nssv2756865
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesAPOBEC3A, APOBEC3A_B, APOBEC3B, APOBEC3B-AS1
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964630
Frequency
Sample Size10
Observed Gain8
Observed Loss1
Observed Complex0
Frequencyn/a


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