A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034556



Internal ID20601596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15729576..15773724hg38UCSC Ensembl
chr17:15632890..15677038hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3844149
hg1944149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511228
Supporting Variants
Samples
Known GenesCDRT15P2, TBC1D26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034556
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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