A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411967



Internal ID22469837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15000393..15001004hg38UCSC Ensembl
chr6:15000624..15001235hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896743
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411967
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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