A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605868



Internal ID16393277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2632431..2659000hg38UCSC Ensembl
Innerchr7:2672065..2698634hg19UCSC Ensembl
Innerchr7:2638591..2665160hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3826570
hg1926570
hg1826570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11145n54
Supporting Variantsnssv1078474
Samples
Known GenesTTYH3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605868
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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