A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155861



Internal ID15880287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:119318926..119493141hg38UCSC Ensembl
Innerchr7:118958980..119133195hg19UCSC Ensembl
Innerchr7:118746216..118920431hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38174216
hg19174216
hg18174216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608317
Supporting Variants
SamplesNINDS_189
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155861
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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