A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607689



Internal ID16048412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:81748600..81781600hg38UCSC Ensembl
Innerchr7:81377916..81410916hg19UCSC Ensembl
Innerchr7:81215852..81248852hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3833001
hg1933001
hg1833001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155219
SamplesHGDP00952
Known GenesHGF
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607689
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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