A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466344



Internal ID22524235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19272799..19276929hg38UCSC Ensembl
chr1:19599293..19603423hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg384131
hg194131
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828491
Supporting Variants
Samples
Known GenesAKR7L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466344
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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