A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118061



Internal ID19261296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:38076702..38076809hg38UCSC Ensembl
Outerchr9:38076699..38076806hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980263
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118061
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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