A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468656



Internal ID22526545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:64339345..64375829hg38UCSC Ensembl
chr10:66099105..66135589hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3836485
hg1936485
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865253
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468656
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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