A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466482



Internal ID22524374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:39319070..39325857hg38UCSC Ensembl
chr12:39712872..39719659hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg386788
hg196788
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848851
Supporting Variants
Samples
Known GenesKIF21A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466482
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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