A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435017



Internal ID22492887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26409030..26409606hg38UCSC Ensembl
chr8:26266546..26267122hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38577
hg19577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5919322
Supporting Variants
Samples
Known GenesBNIP3L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435017
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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