A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927115



Internal ID22702343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6551724..6552306hg38UCSC Ensembl
chr11:6572954..6573536hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv222n209
Supporting Variantsnssv17367417
Samples
Known GenesDNHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927115
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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