A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964833



Internal ID19230984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:75054235..75058816hg38UCSC Ensembl
Outerchr14:75520938..75525519hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg384582
hg194582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111921
Supporting Variants
SamplesKWS2
Known GenesACYP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964833
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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