A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981929



Internal ID18617125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39155490..39158037hg38UCSC Ensembl
Innerchr8:39013009..39015556hg19UCSC Ensembl
Innerchr8:39132166..39134713hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg382548
hg192548
hg182548
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2499663, nssv2499665, nssv2499660, nssv2499661, nssv2499659, nssv2499656, nssv2499657, nssv2499664, nssv2499658, nssv2499662
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesADAM32
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981929
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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