A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17369477



Internal ID22595146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:90811351..90811931hg38UCSC Ensembl
chr10:92571108..92571688hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910469
Supporting Variants
Samples
Known GenesHTR7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17369477
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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