A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367441



Internal ID22593110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101121740..101123600hg38UCSC Ensembl
chr1:101587296..101589156hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg381861
hg191861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876383
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367441
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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