A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139298



Internal ID18912239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:112548818..112549125hg38UCSC Ensembl
Outerchr4:113469974..113470281hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3974473, nssv3956760
SamplesKWS2, KWS1
Known GenesC4orf21
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139298
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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