A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965512



Internal ID22740447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:30994599..31046945hg38UCSC Ensembl
chr21:32366918..32419264hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3852347
hg1952347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404893
Samples
Known GenesKRTAP19-8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965512
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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