A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735060



Internal ID20511000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6801833..6801903hg38UCSC Ensembl
chr10:6843795..6843865hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269596
Samples
Known GenesLINC00707
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735060
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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