A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3996129



Internal ID19190306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:19723597..19728851hg38UCSC Ensembl
Outerchr19:19834406..19839660hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg385255
hg195255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1150655
Supporting Variants
SamplesKWB1
Known GenesZNF14
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3996129
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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