A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734743



Internal ID20510681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:41700745..41700811hg38UCSC Ensembl
chr7:41740343..41740409hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290041
Samples
Known GenesINHBA, INHBA-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734743
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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