A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979891



Internal ID19206727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:2969624..2969721hg38UCSC Ensembl
Outerchr20:2950270..2950367hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143131
Supporting Variants
SamplesKWS1
Known GenesPTPRA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979891
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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