A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17426775



Internal ID22484645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11047637..11047700hg38UCSC Ensembl
chr6:11047870..11047933hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896758
Supporting Variants
Samples
Known GenesELOVL2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17426775
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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