A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132675



Internal ID19266115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:101623072..101624772hg38UCSC Ensembl
Outerchr8:102635300..102637000hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg381701
hg191701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3869n106
Supporting Variantsnssv3987464
SamplesKWS1
Known GenesGRHL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132675
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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