A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743752



Internal ID20519741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6795119..6795250hg38UCSC Ensembl
chr10:6837081..6837212hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268386
Samples
Known GenesLINC00707
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743752
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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