A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037092



Internal ID20604132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61409301..61409900hg38UCSC Ensembl
chr17:59486662..59487261hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520906
Supporting Variants
Samples
Known GenesTBX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037092
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.08533


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