A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516873



Internal ID15097480
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 gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv654612, nssv701204, nssv695205, nssv663029
Samples
Known GenesDLG1, DLG1-AS1, MIR4797
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516873
Frequency
Sample Size2026
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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