A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271033



Internal ID20480251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81078270..81078270hg38UCSC Ensembl
chr17:79052070..79052070hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751458
Supporting Variants
Samples
Known GenesBAIAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271033
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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