A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769872



Internal ID18965848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24832188..24835020hg38UCSC Ensembl
chr1:25158679..25161511hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382833
hg192833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076284
Supporting Variants
SamplesKWP1
Known GenesCLIC4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769872
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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