A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260222



Internal ID20469440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44871118..44871192hg38UCSC Ensembl
chr7:44910717..44910791hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749353
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260222
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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