A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455636



Internal ID22513513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33021241..33029833hg38UCSC Ensembl
chr1:33486842..33495434hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg388593
hg198593
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830294
Supporting Variants
Samples
Known GenesAK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455636
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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