A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990122



Internal ID19233128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:105533572..105534272hg38UCSC Ensembl
Outerchr8:106545800..106546500hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137619
Supporting Variants
SamplesKWS2
Known GenesZFPM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990122
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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