A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134732



Internal ID19260085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:74592789..74592839hg38UCSC Ensembl
Outerchr18:72260025..72260075hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3955395, nssv3972611
SamplesKWS2, KWS1
Known GenesLINC00909
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134732
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer