A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968990



Internal ID18886543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:101896520..101896578hg38UCSC Ensembl
Outerchr14:102362857..102362915hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113672
Supporting Variants
SamplesKWS2
Known GenesPPP2R5C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968990
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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