A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762179



Internal ID18959096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20485506..20486207hg38UCSC Ensembl
chr1:20811999..20812700hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077198
Supporting Variants
SamplesKWP1
Known GenesCAMK2N1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762179
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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