A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17383139



Internal ID22441009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31938743..31945973hg38UCSC Ensembl
chr1:32404344..32411574hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg387231
hg197231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876334
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17383139
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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