A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000837



Internal ID19090054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89186243..90282526hg38UCSC Ensembl
Innerchr2:89485727..90321385hg19UCSC Ensembl
Innerchr2:89266842..89958690hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381096284
hg19835659
hg18691849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582499
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1000837
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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