A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000665



Internal ID19089882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:108601590..108664275hg38UCSC Ensembl
Innerchr3:108320437..108383122hg19UCSC Ensembl
Innerchr3:109803127..109865812hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3862686
hg1962686
hg1862686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604399
Samples
Known GenesDZIP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1000665
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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