A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016698



Internal ID19105915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:179740427..180447834hg38UCSC Ensembl
Innerchr4:180661580..181368987hg19UCSC Ensembl
Innerchr4:180898574..181605981hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38707408
hg19707408
hg18707408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635566
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016698
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer