A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952428



Internal ID17301302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:19723192..19728991hg38UCSC Ensembl
Outerchr19:19834001..19839800hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv80n73
Supporting Variantsnssv2999783
SamplesBILGI_BIOE
Known GenesZNF14
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952428
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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