A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763166



Internal ID18965745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48974954..48999283hg38UCSC Ensembl
chr4:48976971..49001300hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3824330
hg1924330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073757
Supporting Variants
SamplesKWP1
Known GenesCWH43
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763166
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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