A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17410184



Internal ID22468054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134304442..134305778hg38UCSC Ensembl
chr6:134625580..134626916hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg381337
hg191337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905034
Supporting Variants
Samples
Known GenesSGK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17410184
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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