A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010057



Internal ID21919400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124912466..124913479hg38UCSC Ensembl
chr7:124552520..124553533hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg381014
hg191014
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561653
Samples
Known GenesPOT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010057
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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