A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749937



Internal ID20525972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45432585..45432661hg38UCSC Ensembl
chr7:45472184..45472260hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287986
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749937
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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