A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1142037



Internal ID18913258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:14852286..14903469hg38UCSC Ensembl
Outerchr19:14963098..15014281hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3851184
hg1951184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1719n106
Supporting Variantsnssv3993550
SamplesKWS1
Known GenesOR7A17
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1142037
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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