A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367227



Internal ID22592896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7582131..7584561hg38UCSC Ensembl
chr10:7624094..7626524hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382431
hg192431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923263
Supporting Variants
Samples
Known GenesITIH5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367227
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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