A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192986



Internal ID20760027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17286802..17370186hg38UCSC Ensembl
chr17:17190116..17273500hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3883385
hg1983385
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514820
Supporting Variants
Samples
Known GenesNT5M
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192986
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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