A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527560



Internal ID15454853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:200331171..200363077hg38UCSC Ensembl
Innerchr1:200300299..200332205hg19UCSC Ensembl
Innerchr1:198566922..198598828hg18UCSC Ensembl
Innerchr1:197031956..197063862hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3831907
hg1931907
hg1831907
hg1731907
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv23n21
Supporting Variantsnssv704021
Samples
Known GenesLINC00862
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527560
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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