A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17382741



Internal ID22440611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42116595..42116671hg38UCSC Ensembl
chr1:42582266..42582342hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876739
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17382741
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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