A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960330



Internal ID18863993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:144602626..144602804hg38UCSC Ensembl
Outerchr8:145828010..145828188hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128461
Supporting Variants
SamplesKWS1
Known GenesARHGAP39
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960330
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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