A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17440247



Internal ID22498117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105380601..105380704hg38UCSC Ensembl
chr8:106392829..106392932hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5914617
Supporting Variants
Samples
Known GenesZFPM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17440247
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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