A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037867



Internal ID20604907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6578801..6579061hg38UCSC Ensembl
chr17:6482121..6482381hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514684
Supporting Variants
Samples
Known GenesKIAA0753
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037867
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00033


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