A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1084629



Internal ID15937815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:53383163..53522557hg38UCSC Ensembl
Innerchr7:53450856..53590250hg19UCSC Ensembl
Innerchr7:53418350..53557744hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38139395
hg19139395
hg18139395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607011
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1084629
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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