A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735656



Internal ID20511600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26572111..26624739hg38UCSC Ensembl
chr10:26861040..26913668hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3852629
hg1952629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277776
Samples
Known GenesLINC00264
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735656
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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