A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295614



Internal ID20504832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31316044..31316237hg38UCSC Ensembl
chr16:31327365..31327558hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736600
Supporting Variants
Samples
Known GenesITGAM
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295614
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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