A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000140



Internal ID18742671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:154618472..155187951hg38UCSC Ensembl
Innerchr3:154336261..154905740hg19UCSC Ensembl
Innerchr3:155818955..156388434hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38569480
hg19569480
hg18569480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3741548
Samples
Known GenesMME
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1000140
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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