A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364448



Internal ID22590117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34007785..34008073hg38UCSC Ensembl
chr11:34029332..34029620hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926398
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364448
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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