A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070659



Internal ID19317769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19723490..19728891hg38UCSC Ensembl
chr19:19834299..19839700hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg385402
hg195402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763638
SamplesKWP1
Known GenesZNF14
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070659
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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