A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011522



Internal ID18754056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62800051..62846555hg38UCSC Ensembl
Innerchr3:62785726..62832230hg19UCSC Ensembl
Innerchr3:62760766..62807270hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3846505
hg1946505
hg1846505
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3594574
Samples
Known GenesCADPS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011522
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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