A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1092683



Internal ID15599183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110662639..110702868hg38UCSC Ensembl
Innerchr7:110302695..110342924hg19UCSC Ensembl
Innerchr7:110089931..110130160hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3840230
hg1940230
hg1840230
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608148
Supporting Variants
Samples
Known GenesIMMP2L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1092683
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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