A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524992



Internal ID15105599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:91175510..91176712hg38UCSC Ensembl
Innerchr8:92187738..92188940hg19UCSC Ensembl
Innerchr8:92256914..92258116hg18UCSC Ensembl
Innerchr8:92256914..92258116hg17UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg381203
hg191203
hg181203
hg171203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701021
Samples
Known GenesLRRC69
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524992
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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