A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17571581



Internal ID21763624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53287129..53287485hg38UCSC Ensembl
chr6:53151927..53152283hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001248
Supporting Variants
Samples
Known GenesELOVL5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17571581
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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