A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17642102



Internal ID21834149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:15030888..15031687hg38UCSC Ensembl
chr21:16403209..16404008hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6053554
Supporting Variants
Samples
Known GenesNRIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17642102
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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