A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967363



Internal ID19211085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:56365905..56366003hg38UCSC Ensembl
Outerchr20:54940961..54941059hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136555
Supporting Variants
SamplesKWS1
Known GenesFAM210B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967363
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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