A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953612



Internal ID16955799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:53978147..53994046hg38UCSC Ensembl
Outerchr19:54481401..54497300hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3815900
hg1915900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999878
SamplesBILGI_BIOE
Known GenesCACNG6, CACNG8, MIR935
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953612
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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