A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771662



Internal ID19314587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1572353..1613554hg38UCSC Ensembl
chr20:1552999..1594200hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3841202
hg1941202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071672
Supporting Variants
SamplesKWP1
Known GenesSIRPB1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771662
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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