A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523874



Internal ID20897235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17431714..17436348hg38UCSC Ensembl
chr19:17542523..17547157hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg384635
hg194635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045184
Samples
Known GenesTMEM221
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523874
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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