A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971045



Internal ID18606267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97935263..97938847hg38UCSC Ensembl
Innerchr7:97564575..97568159hg19UCSC Ensembl
Innerchr7:97402511..97406095hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg383585
hg193585
hg183585
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2719331, nssv2719334, nssv2719333, nssv2719330, nssv2719332, nssv2719335, nssv2719329, nssv2719337, nssv2719338, nssv2719336
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971045
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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