A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607703



Internal ID16395112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:83188068..83213101hg38UCSC Ensembl
Innerchr7:82817384..82842417hg19UCSC Ensembl
Innerchr7:82655320..82680353hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3825034
hg1925034
hg1825034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155224
SamplesHGDP00909
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607703
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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