A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006359



Internal ID19095576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:29459991..29501317hg38UCSC Ensembl
Innerchr2:29682857..29724183hg19UCSC Ensembl
Innerchr2:29536361..29577687hg18UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg3841327
hg1941327
hg1841327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3727992
Samples
Known GenesALK
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006359
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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