A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352602



Internal ID22578271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23508778..23508841hg38UCSC Ensembl
chr1:23835270..23835333hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875435
Supporting Variants
Samples
Known GenesE2F2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352602
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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