A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979822



Internal ID18615023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:40698270..40701583hg38UCSC Ensembl
Innerchr3:40739761..40743074hg19UCSC Ensembl
Innerchr3:40714765..40718078hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg383314
hg193314
hg183314
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2280752, nssv2280755, nssv2280754, nssv2280757, nssv2280756, nssv2280751, nssv2280758, nssv2280759, nssv2280753, nssv2280750
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv979822
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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