A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277776



Internal ID20486994
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 StatusS
Merged Variantsnsv4735656
Supporting Variants
Samples
Known GenesLINC00264
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277776
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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