A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953580



Internal ID16955767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:41888230..41997948hg38UCSC Ensembl
Outerchr19:42392301..42502100hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38109719
hg19109800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999846
SamplesBILGI_BIOE
Known GenesARHGEF1, ATP1A3, RABAC1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953580
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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