A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702937



Internal ID15439589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29603768..29608616hg38UCSC Ensembl
Innerchr6:29571545..29576393hg19UCSC Ensembl
Innerchr6:29679524..29684372hg18UCSC Ensembl
Innerchr6:29679524..29684372hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg384849
hg194849
hg184849
hg174849
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526617
Supporting Variants
Samples
Known GenesGABBR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702937
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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