A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1123831



Internal ID18919079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:112622345..112622409hg38UCSC Ensembl
Outerchr4:113543501..113543565hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3973994
SamplesKWS2
Known GenesC4orf21
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1123831
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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