A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143574



Internal ID18909983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:11014239..11014338hg38UCSC Ensembl
Outerchr18:11014237..11014336hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980784
SamplesKWS1
Known GenesPIEZO2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143574
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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