A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564693



Internal ID18516288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11151554..11232027hg38UCSC Ensembl
Innerchr19:11262230..11342703hg19UCSC Ensembl
Innerchr19:11123230..11203703hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3880474
hg1980474
hg1880474
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057712
Supporting Variants
Samples
Known GenesDOCK6, KANK2, SPC24
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564693
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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