A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294879



Internal ID20504097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76292161..76292254hg38UCSC Ensembl
chr17:74288242..74288335hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739018
Supporting Variants
Samples
Known GenesQRICH2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294879
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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