A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1088528



Internal ID15595028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79681270..79805427hg38UCSC Ensembl
Innerchr7:79310586..79434743hg19UCSC Ensembl
Innerchr7:79148522..79272679hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38124158
hg19124158
hg18124158
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607670
Supporting Variants
Samples
Known GenesMIR548M
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1088528
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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