A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795929



Internal ID21241268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57218711..57219033hg38UCSC Ensembl
chr16:57252623..57252945hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13684010
Samples
Known GenesRSPRY1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795929
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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