A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266256



Internal ID20475474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15791203..15791284hg38UCSC Ensembl
chr4:15792826..15792907hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749108
Supporting Variants
Samples
Known GenesCD38
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266256
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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