A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989400



Internal ID18887260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:99520490..99520542hg38UCSC Ensembl
Outerchr14:99986827..99986879hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1135811
Supporting Variants
SamplesKWS2
Known GenesCCDC85C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989400
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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