A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18038252



Internal ID20605292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76694031..76697062hg38UCSC Ensembl
chr17:74690113..74693144hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg383032
hg193032
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520303
Supporting Variants
Samples
Known GenesMXRA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18038252
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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