A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901356



Internal ID15848626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54053501..54058538hg38UCSC Ensembl
Innerchr19:54556755..54561792hg19UCSC Ensembl
Innerchr19:59248567..59253604hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg385038
hg195038
hg185038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580137
Supporting Variants
Samples
Known GenesVSTM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901356
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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