A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3955056



Internal ID18865132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:44965961..44966024hg38UCSC Ensembl
Outerchr14:45435164..45435227hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1127379
Supporting Variants
SamplesKWS1
Known GenesFAM179B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3955056
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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