A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950380



Internal ID16952567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:112577045..112580444hg38UCSC Ensembl
Outerchr4:113498201..113501600hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996766
SamplesBILGI_BIOE
Known GenesC4orf21
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950380
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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