A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625987



Internal ID15849520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:74416504..74416870hg38UCSC Ensembl
Outerchr7:74416387..74423185hg38UCSC Ensembl
Innerchr7:73830834..73831200hg19UCSC Ensembl
Outerchr7:73830717..73837515hg19UCSC Ensembl
Innerchr7:73468770..73469136hg18UCSC Ensembl
Outerchr7:73468653..73475451hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg386799
hg196799
hg186799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511381
Supporting Variants
Samples1
Known Genes
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625987
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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