A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276368



Internal ID20485586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24668150..24668150hg38UCSC Ensembl
chr1:24994641..24994641hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756596
Supporting Variants
Samples
Known GenesSRRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276368
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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