A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1083632



Internal ID15936818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:44960916..44969364hg38UCSC Ensembl
Innerchr7:45000515..45008963hg19UCSC Ensembl
Innerchr7:44967040..44975488hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg388449
hg198449
hg188449
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606828
Supporting Variants
Samples
Known GenesMYO1G
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1083632
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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