A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979091



Internal ID19222438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:12397128..12436911hg38UCSC Ensembl
Outerchr19:12507942..12547725hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3839784
hg1939784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140383
Supporting Variants
SamplesKWS1
Known GenesZNF443, ZNF799
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979091
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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