A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451902



Internal ID22509774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111889766..111904628hg38UCSC Ensembl
chr1:112432388..112447250hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3814863
hg1914863
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5827805
Supporting Variants
Samples
Known GenesKCND3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451902
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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