A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109684



Internal ID19249136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:61033352..61033464hg38UCSC Ensembl
Outerchr8:61945911..61946023hg19UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3833n106
Supporting Variantsnssv3957252
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109684
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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