A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035660



Internal ID20602700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42876597..42878965hg38UCSC Ensembl
chr17:41028614..41030982hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg382369
hg192369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514464
Supporting Variants
Samples
Known GenesLINC00671
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035660
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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