A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518945



Internal ID15446238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27666861..27700234hg38UCSC Ensembl
Innerchr6:27634640..27668013hg19UCSC Ensembl
Innerchr6:27742619..27775992hg18UCSC Ensembl
Innerchr6:27742619..27775992hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3833374
hg1933374
hg1833374
hg1733374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694291
Samples
Known GenesLINC01012
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518945
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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