A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3530996



Internal ID18829277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48315557..48444284hg38UCSC Ensembl
Innerchr14:48784760..48913487hg19UCSC Ensembl
Innerchr14:47854510..47983237hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38128728
hg19128728
hg18128728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050803
Supporting Variants
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)nssv3530996
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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