A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970900



Internal ID18606122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:77116369..77182061hg38UCSC Ensembl
Innerchr7:76745686..76811378hg19UCSC Ensembl
Innerchr7:76583622..76649314hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3865693
hg1965693
hg1865693
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2467864, nssv2467871, nssv2467869, nssv2467863, nssv2467868, nssv2467865, nssv2467870, nssv2467866, nssv2467867, nssv2467862
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCCDC146
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970900
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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