A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145252



Internal ID20712292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76102961..76186514hg38UCSC Ensembl
chr6:76812678..76896231hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3883554
hg1983554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403632
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145252
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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