A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3955483



Internal ID18874531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:58459048..58487034hg38UCSC Ensembl
Outerchr19:58970415..58998401hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3827987
hg1927987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116353
Supporting Variants
SamplesKWS1
Known GenesZNF324, ZNF446
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3955483
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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