A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455755



Internal ID22513632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45792280..45807440hg38UCSC Ensembl
chr10:46287728..46302888hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3815161
hg1915161
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858577
Supporting Variants
Samples
Known GenesFAM21C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455755
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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