A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292607



Internal ID20501825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29537701..29537701hg38UCSC Ensembl
chr19:30028608..30028608hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763470
Supporting Variants
Samples
Known GenesVSTM2B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292607
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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