A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1116277



Internal ID19282069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:61616629..61616865hg38UCSC Ensembl
Outerchr18:59283862..59284098hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3954634
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1116277
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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