A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001690



Internal ID19090907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:235328077..235352880hg38UCSC Ensembl
Innerchr2:236236721..236261524hg19UCSC Ensembl
Innerchr2:235901460..235926263hg18UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg3824804
hg1924804
hg1824804
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3586950
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)nsv1001690
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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