A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515988



Internal ID15443045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:24454451..24463233hg38UCSC Ensembl
Innerchr6:24454679..24463461hg19UCSC Ensembl
Innerchr6:24562658..24571440hg18UCSC Ensembl
Innerchr6:24562658..24571440hg17UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg388783
hg198783
hg188783
hg178783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665598, nssv696331, nssv657851, nssv660217
Samples
Known GenesGPLD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515988
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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