A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18038212



Internal ID20605252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76298160..76300082hg38UCSC Ensembl
chr17:74294241..74296163hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381923
hg191923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531970
Supporting Variants
Samples
Known GenesQRICH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18038212
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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