A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525990



Internal ID15106597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160482590..160549931hg38UCSC Ensembl
Innerchr6:160903622..160970963hg19UCSC Ensembl
Innerchr6:160823612..160890953hg18UCSC Ensembl
Innerchr6:160874033..160941374hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3867342
hg1967342
hg1867342
hg1767342
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702212
Samples
Known GenesLPA, LPAL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525990
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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