A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517362



Internal ID15444655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19735649..19761284hg38UCSC Ensembl
Innerchr19:19846458..19872093hg19UCSC Ensembl
Innerchr19:19707458..19733093hg18UCSC Ensembl
Innerchr19:19707458..19733093hg17UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3825636
hg1925636
hg1825636
hg1725636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv693634, nssv685371, nssv654696, nssv651818
Samples
Known GenesLINC00663
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517362
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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