A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008675



Internal ID19097892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:234093597..234113080hg38UCSC Ensembl
Innerchr2:235002241..235021724hg19UCSC Ensembl
Innerchr2:234666980..234686463hg18UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3819484
hg1919484
hg1819484
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3586942
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)nsv1008675
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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