A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971044



Internal ID18606266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97924268..97934763hg38UCSC Ensembl
Innerchr7:97553580..97564075hg19UCSC Ensembl
Innerchr7:97391516..97402011hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3810496
hg1910496
hg1810496
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2719259, nssv2719264, nssv2719263, nssv2719262, nssv2719260, nssv2719265, nssv2719261, nssv2719266, nssv2719268, nssv2719267
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)nsv971044
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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