A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037225



Internal ID20604265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63201265..63201665hg38UCSC Ensembl
chr17:61278626..61279026hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521418
Supporting Variants
Samples
Known GenesTANC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037225
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00086


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