A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984610



Internal ID18875308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:75428097..75428397hg38UCSC Ensembl
Outerchr14:75894800..75895100hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126368
Supporting Variants
SamplesKWS1
Known GenesJDP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984610
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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