A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960054



Internal ID18873538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:36349798..36356198hg38UCSC Ensembl
Outerchr19:36840700..36847100hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg386401
hg196401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110403
Supporting Variants
SamplesKWS1
Known GenesZFP14
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960054
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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