A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002454



Internal ID21911797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36343398..36343529hg38UCSC Ensembl
chr7:36383007..36383138hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571543
Samples
Known GenesKIAA0895
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002454
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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