A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388086



Internal ID22445956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90032692..90034111hg38UCSC Ensembl
chr15:90575924..90577343hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381420
hg191420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931998
Supporting Variants
Samples
Known GenesZNF710
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388086
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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