A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703885



Internal ID15440537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:89285232..89289577hg38UCSC Ensembl
Innerchr6:89994951..89999296hg19UCSC Ensembl
Innerchr6:90051670..90056015hg18UCSC Ensembl
Innerchr6:90051670..90056015hg17UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg384346
hg194346
hg184346
hg174346
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527444
Supporting Variants
Samples
Known GenesGABRR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703885
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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