A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515221



Internal ID20888580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30793961..30794384hg38UCSC Ensembl
chr17:29120979..29121402hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38424
hg19424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035417
Samples
Known GenesCRLF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515221
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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