A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1078471



Internal ID15931657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2612996..2655983hg38UCSC Ensembl
Innerchr7:2652630..2695617hg19UCSC Ensembl
Innerchr7:2619156..2662143hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3842988
hg1942988
hg1842988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605863
Supporting Variants
Samples
Known GenesIQCE, TTYH3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1078471
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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