A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1100267



Internal ID15606767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155291183..155308145hg38UCSC Ensembl
Innerchr7:155082893..155099855hg19UCSC Ensembl
Innerchr7:154713826..154730788hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3816963
hg1916963
hg1816963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609126
Supporting Variants
Samples
Known GenesINSIG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1100267
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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