A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535536



Internal ID20908897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11488856..11491808hg38UCSC Ensembl
chr19:11599671..11602623hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382953
hg192953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045008
Samples
Known GenesZNF653
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535536
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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