A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606554



Internal ID20979625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44944773..44946343hg38UCSC Ensembl
chr7:44984372..44985942hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg381571
hg191571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154634
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606554
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