A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037273



Internal ID21946616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10068255..10068309hg38UCSC Ensembl
chr17:9971572..9971626hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618488
Samples
Known GenesGAS7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037273
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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