A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1070795



Internal ID15923981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:101862851..101902872hg38UCSC Ensembl
Innerchr6:102310726..102350747hg19UCSC Ensembl
Innerchr6:102417419..102457440hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3840022
hg1940022
hg1840022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604320
Supporting Variants
Samples
Known GenesGRIK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1070795
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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