A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261254



Internal ID20470472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:123996880..123997213hg38UCSC Ensembl
chr7:123636934..123637267hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745667
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261254
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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