A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607471



Internal ID20980542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81712199..81714524hg38UCSC Ensembl
chr7:81341515..81343840hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg382326
hg192326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160236
Samples
Known GenesHGF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607471
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