A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv982572



Internal ID16276528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:183825041..183825817hg38UCSC Ensembl
Innerchr3:183542829..183543605hg19UCSC Ensembl
Innerchr3:185025523..185026299hg18UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38777
hg19777
hg18777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592665
Supporting Variants
Samples
Known GenesMAP6D1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv982572
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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