A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035656



Internal ID20602696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42827801..42829216hg38UCSC Ensembl
chr17:40979818..40981233hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381416
hg191416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512148
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035656
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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