A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702482



Internal ID15439134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:14279120..14283796hg38UCSC Ensembl
Innerchr6:14279351..14284027hg19UCSC Ensembl
Innerchr6:14387330..14392006hg18UCSC Ensembl
Innerchr6:14387330..14392006hg17UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg384677
hg194677
hg184677
hg174677
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526218
Supporting Variants
Samples
Known GenesLINC01108
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702482
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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