A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970788



Internal ID18606010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5918314..5918814hg38UCSC Ensembl
Innerchr7:5957945..5958445hg19UCSC Ensembl
Innerchr7:5924471..5924971hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2433765, nssv2433768, nssv2433759, nssv2433760, nssv2433764, nssv2433762, nssv2433763, nssv2433761, nssv2433766, nssv2433767
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCCZ1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970788
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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