A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242633



Internal ID20809673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64086665..64089188hg38UCSC Ensembl
chr17:62164025..62166548hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg382524
hg192524
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577551
Supporting Variants
Samples
Known GenesERN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242633
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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