A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281236



Internal ID20490454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81610336..81610336hg38UCSC Ensembl
chr7:81239652..81239652hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751445
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281236
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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