A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3565652



Internal ID18517247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:66417321..66663853hg38UCSC Ensembl
Innerchr18:64084558..64331090hg19UCSC Ensembl
Innerchr18:62235538..62482070hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38246533
hg19246533
hg18246533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058812
Supporting Variants
Samples
Known GenesCDH19
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3565652
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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