A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357788



Internal ID22583457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11773129..11775374hg38UCSC Ensembl
chr10:11815128..11817373hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382246
hg192246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5914924
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357788
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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