A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762402



Internal ID18964499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112548823..112549142hg38UCSC Ensembl
chr4:113469979..113470298hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073366
Supporting Variants
SamplesKWP1
Known GenesC4orf21
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762402
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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