A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603761



Internal ID20976832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27288690..27295976hg38UCSC Ensembl
chr7:27328309..27335595hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg387287
hg197287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157014
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603761
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