A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969273



Internal ID19227662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:142510439..142511139hg38UCSC Ensembl
Outerchr8:143591800..143592500hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133701
Supporting Variants
SamplesKWS2
Known GenesBAI1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969273
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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