A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953561



Internal ID17302435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:76401845..76409444hg38UCSC Ensembl
Outerchr18:74113801..74121400hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg387600
hg197600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998896
SamplesBILGI_BIOE
Known GenesZNF516
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953561
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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