A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155120



Internal ID15531558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3154523..3309993hg38UCSC Ensembl
Innerchr7:3194156..3349625hg19UCSC Ensembl
Innerchr7:3160682..3316151hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38155471
hg19155470
hg18155470
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605880
Supporting Variants
SamplesHGDP01166
Known GenesSDK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155120
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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