A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037191



Internal ID20604231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62701168..62702372hg38UCSC Ensembl
chr17:60778529..60779733hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg381205
hg191205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534060
Supporting Variants
Samples
Known GenesMARCH10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037191
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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