A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3532246



Internal ID18830527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22194962..22500001hg38UCSC Ensembl
Innerchr14:22662856..22968984hg19UCSC Ensembl
Innerchr14:21732696..22038824hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38305040
hg19306129
hg18306129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048895
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)nssv3532246
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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