A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034676



Internal ID20601716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29176501..29177100hg38UCSC Ensembl
chr17:27503519..27504118hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510317
Supporting Variants
Samples
Known GenesMYO18A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034676
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01719


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