A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3532636



Internal ID18830917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:97661651..97681388hg38UCSC Ensembl
Innerchr14:98127988..98147725hg19UCSC Ensembl
Innerchr14:97197741..97217478hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3819738
hg1919738
hg1819738
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048157
Supporting Variants
Samples
Known GenesLOC100129345
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3532636
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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