A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002245



Internal ID21911588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143420826..143448539hg38UCSC Ensembl
chr7:143117919..143145632hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3827714
hg1927714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561780
Samples
Known GenesEPHA1-AS1, TAS2R60
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002245
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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