A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067270



Internal ID21976503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128107605..128107605hg38UCSC Ensembl
chr7:127747657..127747657hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571222
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067270
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer