A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455268



Internal ID22513145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4724321..4727518hg38UCSC Ensembl
chr10:4766513..4769710hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg383198
hg193198
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860607
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455268
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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