A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002836



Internal ID19092053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:139628219..139716308hg38UCSC Ensembl
Innerchr2:140385788..140473877hg19UCSC Ensembl
Innerchr2:140102258..140190347hg18UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3888090
hg1988090
hg1888090
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582803
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)nsv1002836
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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