A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522353



Internal ID15102960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:66576761..66580904hg38UCSC Ensembl
Innerchr2:66803893..66808036hg19UCSC Ensembl
Innerchr2:66657397..66661540hg18UCSC Ensembl
Innerchr2:66715544..66719687hg17UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg384144
hg194144
hg184144
hg174144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695132
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522353
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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