A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366602



Internal ID22592271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:190638858..190775385hg38UCSC Ensembl
chr1:190607988..190744515hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38136528
hg19136528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868211
Supporting Variants
Samples
Known GenesLOC440704
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366602
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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