A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522457



Internal ID15449750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5244837..5260703hg38UCSC Ensembl
Innerchr6:5245070..5260936hg19UCSC Ensembl
Innerchr6:5190069..5205935hg18UCSC Ensembl
Innerchr6:5190069..5205935hg17UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3815867
hg1915867
hg1815867
hg1715867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705820
Samples
Known GenesLYRM4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522457
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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