A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999797



Internal ID19159333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89200973..90228225hg38UCSC Ensembl
Innerchr2:89500461..90267091hg19UCSC Ensembl
Innerchr2:89281576..89904396hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381027253
hg19766631
hg18622821
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3965n100
Supporting Variantsnssv3582506, nssv3582507
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)nsv999797
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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