A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605870



Internal ID16393279
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 StatusM
Merged Variants
Supporting Variantsnssv1078475
Samples
Known GenesTTYH3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605870
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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