A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739007



Internal ID20514979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121648763..121649496hg38UCSC Ensembl
chr7:121288817..121289550hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265078
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739007
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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