A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762828



Internal ID19313289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150718974..150719292hg38UCSC Ensembl
chr1:150691450..150691768hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078810
Supporting Variants
SamplesKWP1
Known GenesHORMAD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762828
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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