A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606618



Internal ID16047341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:36577662..36792118hg38UCSC Ensembl
Innerchr7:36617268..36831723hg19UCSC Ensembl
Innerchr7:36583793..36798248hg18UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38214457
hg19214456
hg18214456
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155166
SamplesHGDP01077
Known GenesAOAH, AOAH-IT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606618
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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