A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17358384



Internal ID22584053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161579290..161661012hg38UCSC Ensembl
chr1:161549080..161630802hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3881723
hg1981723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880515
Supporting Variants
Samples
Known GenesFCGR2C, FCGR3B, HSPA7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17358384
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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