A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970534



Internal ID18605756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:74969837..74973701hg38UCSC Ensembl
Innerchr7:74383987..74387851hg19UCSC Ensembl
Innerchr7:74021923..74025787hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg383865
hg193865
hg183865
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2463277, nssv2463274, nssv2463278, nssv2463280, nssv2463272, nssv2463276, nssv2463273, nssv2463281, nssv2463279, nssv2463275
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970534
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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