A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945851



Internal ID18592701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:27649352..27650502hg38UCSC Ensembl
Innerchr1:27975863..27977013hg19UCSC Ensembl
Innerchr1:27848450..27849600hg18UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381151
hg191151
hg181151
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1757280, nssv1757271, nssv1757272, nssv1757279, nssv1757277, nssv1757274, nssv1757276, nssv1757278, nssv1757275, nssv1757273
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)nsv945851
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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