A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109119



Internal ID18912937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:10795315..10795390hg38UCSC Ensembl
Outerchr18:10795313..10795388hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3954970
SamplesKWS1
Known GenesPIEZO2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109119
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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