A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135385



Internal ID20702426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110847301..110848400hg38UCSC Ensembl
chr6:111168504..111169603hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610896
Supporting Variants
Samples
Known GenesAMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135385
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00355


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