A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654612



Internal ID15044578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:197066987..197300056hg38UCSC Ensembl
Innerchr3:196793858..197026927hg19UCSC Ensembl
Innerchr3:198278255..198511324hg18UCSC Ensembl
Innerchr3:198282168..198515237hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38233070
hg19233070
hg18233070
hg17233070
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516873
Supporting Variants
Samples
Known GenesDLG1, DLG1-AS1, MIR4797
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654612
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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