A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970959



Internal ID18606181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148580420..148581660hg38UCSC Ensembl
Innerchr7:148277512..148278752hg19UCSC Ensembl
Innerchr7:147908445..147909685hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg381241
hg191241
hg181241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2486302, nssv2486304, nssv2486305, nssv2486311, nssv2486307, nssv2486308, nssv2486309, nssv2486306, nssv2486310, nssv2486303
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)nsv970959
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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