A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1086550



Internal ID15939736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:72279911..72517939hg38UCSC Ensembl
Innerchr7:71744896..71982924hg19UCSC Ensembl
Innerchr7:71382832..71620860hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38238029
hg19238029
hg18238029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607461
Supporting Variants
Samples
Known GenesCALN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1086550
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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