A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003983



Internal ID21913326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37299033..37306120hg38UCSC Ensembl
chr9:37299030..37306117hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg387088
hg197088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591823
Samples
Known GenesZCCHC7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003983
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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