A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616407



Internal ID20989478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:83686595..83689810hg38UCSC Ensembl
chr7:83315911..83319126hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg383216
hg193216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161642
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616407
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