A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762431



Internal ID19314799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201023571..201024072hg38UCSC Ensembl
chr1:200992699..200993200hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069197
Supporting Variants
SamplesKWP1
Known GenesKIF21B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762431
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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