A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281361



Internal ID20490579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157122250..157127001hg38UCSC Ensembl
chr7:156914944..156919695hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg384752
hg194752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732132
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281361
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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