A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1142021



Internal ID19254600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:6152342..6152549hg38UCSC Ensembl
Outerchr19:6152353..6152560hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1698n106
Supporting Variantsnssv3993535
SamplesKWS1
Known GenesACSBG2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1142021
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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