A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524696



Internal ID15451989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143087674..143093513hg38UCSC Ensembl
Innerchr8:144169091..144174930hg19UCSC Ensembl
Innerchr8:144240466..144246305hg18UCSC Ensembl
Innerchr8:144240466..144246305hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg385840
hg195840
hg185840
hg175840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700675
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524696
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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