A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197617



Internal ID20764657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6885411..6972916hg38UCSC Ensembl
chr18:6885410..6972915hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3887506
hg1987506
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534298
Supporting Variants
Samples
Known GenesARHGAP28, LAMA1, LINC00668
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197617
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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