A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17443141



Internal ID22501011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3181807..3182298hg38UCSC Ensembl
chr6:3182041..3182532hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38492
hg19492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897295
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17443141
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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