A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003607



Internal ID21912950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:50708263..50708352hg38UCSC Ensembl
chr6:50675976..50676065hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560883
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003607
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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