A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739532



Internal ID20515505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36313055..36313141hg38UCSC Ensembl
chr7:36352664..36352750hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277099
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739532
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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