A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141251



Internal ID20708291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148865211..148869425hg38UCSC Ensembl
chr6:149186347..149190561hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg384215
hg194215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607941
Supporting Variants
Samples
Known GenesUST
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141251
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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