A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138689



Internal ID20705729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125700452..125700829hg38UCSC Ensembl
chr6:126021598..126021975hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606270
Supporting Variants
Samples
Known GenesLOC643623
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138689
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00096


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