A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981605



Internal ID18616802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149190894..149191777hg38UCSC Ensembl
Innerchr7:148887986..148888869hg19UCSC Ensembl
Innerchr7:148518919..148519802hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38884
hg19884
hg18884
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2486564, nssv2486563, nssv2486567, nssv2486558, nssv2486560, nssv2486565, nssv2486562, nssv2486561, nssv2486559, nssv2486566
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)nsv981605
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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