A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531685



Internal ID18829966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:47757822..47807906hg38UCSC Ensembl
Innerchr14:48227025..48277109hg19UCSC Ensembl
Innerchr14:47296775..47346859hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3850085
hg1950085
hg1850085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047157
Supporting Variants
Samples
Known GenesLINC00648, MIR548Y
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3531685
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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