A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703073



Internal ID15439725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:89286686..89296206hg38UCSC Ensembl
Innerchr6:89996405..90005925hg19UCSC Ensembl
Innerchr6:90053124..90062644hg18UCSC Ensembl
Innerchr6:90053124..90062644hg17UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg389521
hg199521
hg189521
hg179521
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526732
Supporting Variants
Samples
Known GenesGABRR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703073
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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