A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv464429



Internal ID15177808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:37102969..37105403hg38UCSC Ensembl
Innerchr7:37142574..37145008hg19UCSC Ensembl
Innerchr7:37109099..37111533hg18UCSC Ensembl
Innerchr7:36915814..36918248hg17UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg382435
hg192435
hg182435
hg172435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv810n27
Supporting Variantsnssv540347
SamplesHGDP00541
Known GenesELMO1
MethodSNP array
AnalysisAn HMM examining LogR Ratio and B-allele Frequency was used to classify SNP array data into regions of copy-number 0-3. A combination of manual and automated curation was used on the resulting output to reduce false positives.
PlatformNot reported
Comments
ReferenceItsara_et_al_2009
Pubmed ID19166990
Accession Number(s)nsv464429
Frequency
Sample Size1557
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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