A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606001



Internal ID20979072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55277549..55285082hg38UCSC Ensembl
chr7:55345242..55352775hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg387534
hg197534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159220
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606001
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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