A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527868



Internal ID15455161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:10253956..10255818hg38UCSC Ensembl
Innerchr2:10394082..10395944hg19UCSC Ensembl
Innerchr2:10311533..10313395hg18UCSC Ensembl
Innerchr2:10344680..10346542hg17UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381863
hg191863
hg181863
hg171863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704367
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527868
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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