A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275885



Internal ID20485103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:74561064..74561064hg38UCSC Ensembl
chr2:74788191..74788191hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750655
Supporting Variants
Samples
Known GenesM1AP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275885
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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