A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732132



Internal ID20508055
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 StatusM
Merged Variants
Supporting Variantsnssv16281361
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732132
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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