A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967480



Internal ID18602708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97756130..97772558hg38UCSC Ensembl
Innerchr7:97385442..97401870hg19UCSC Ensembl
Innerchr7:97223378..97239806hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3816429
hg1916429
hg1816429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2765117, nssv2757723
SamplesHGDP00998, HGDP00778
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967480
Frequency
Sample Size10
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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