A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124373



Internal ID19265319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:123265031..123265096hg38UCSC Ensembl
Outerchr8:124277271..124277336hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3975673
SamplesKWS2
Known GenesZHX1, ZHX1-C8ORF76
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124373
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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