A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380680



Internal ID22438550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41003395..41003532hg38UCSC Ensembl
chr13:41577531..41577668hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5937519
Supporting Variants
Samples
Known GenesELF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380680
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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