A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435975



Internal ID22493845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24806472..24809714hg38UCSC Ensembl
chr6:24806700..24809942hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg383243
hg193243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5891546
Supporting Variants
Samples
Known GenesFAM65B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435975
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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