A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126476



Internal ID18934506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:10454303..10455103hg38UCSC Ensembl
Outerchr18:10454300..10455100hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984727
SamplesKWS1
Known GenesAPCDD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126476
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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