A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367004



Internal ID22592673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:188523855..188542708hg38UCSC Ensembl
chr1:188492986..188511839hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3818854
hg1918854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882647
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367004
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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