A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1078475



Internal ID15931661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2639815..2669580hg38UCSC Ensembl
Innerchr7:2679449..2709214hg19UCSC Ensembl
Innerchr7:2645975..2675740hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3829766
hg1929766
hg1829766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605870
Supporting Variants
Samples
Known GenesTTYH3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1078475
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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