A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155862



Internal ID15853979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:125063702..125165225hg38UCSC Ensembl
Innerchr7:124703756..124805279hg19UCSC Ensembl
Innerchr7:124490992..124592515hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38101524
hg19101524
hg18101524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608344
Supporting Variants
Samples1780854496_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155862
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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