A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113663



Internal ID19253463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:74349280..74349337hg38UCSC Ensembl
Outerchr14:74815983..74816040hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3968979, nssv3970919
SamplesKWS2, KWS1
Known GenesVRTN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113663
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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