A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529405



Internal ID20902766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37878807..37896858hg38UCSC Ensembl
chr19:38369447..38387498hg19UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg3818052
hg1918052
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046686
Samples
Known GenesWDR87
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529405
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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