A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525481



Internal ID15452774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:157731299..157776294hg38UCSC Ensembl
Innerchr6:158152331..158197326hg19UCSC Ensembl
Innerchr6:158072319..158117314hg18UCSC Ensembl
Innerchr6:158122740..158167735hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3844996
hg1944996
hg1844996
hg1744996
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701609
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525481
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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