A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522578



Internal ID15449871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:150547307..150552630hg38UCSC Ensembl
Innerchr6:150868443..150873766hg19UCSC Ensembl
Innerchr6:150910136..150915459hg18UCSC Ensembl
Innerchr6:150960557..150965880hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg385324
hg195324
hg185324
hg175324
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705965
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522578
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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