A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415489



Internal ID22473359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:124847965..124849328hg38UCSC Ensembl
chr6:125169111..125170474hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg381364
hg191364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901335
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415489
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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