A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18150477



Internal ID20717517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96519903..96521081hg38UCSC Ensembl
chr6:96967779..96968957hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg381179
hg191179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602165
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18150477
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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