A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv712329



Internal ID15659599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:36692344..36841680hg38UCSC Ensembl
Innerchr1:37157945..37307281hg19UCSC Ensembl
Innerchr1:36930532..37079868hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38149337
hg19149337
hg18149337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546001
Supporting Variants
Samples
Known GenesGRIK3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv712329
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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