A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003330



Internal ID21912673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7271990..7272220hg38UCSC Ensembl
chr6:7272223..7272453hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572152
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003330
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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