A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18150448



Internal ID20717488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96263713..96269927hg38UCSC Ensembl
chr6:96711589..96717803hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg386215
hg196215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414732
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18150448
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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