A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743313



Internal ID20519301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156133496..156133587hg38UCSC Ensembl
chr7:155926190..155926281hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288899
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743313
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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