A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605498



Internal ID20978569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113187701..113191400hg38UCSC Ensembl
chr7:112827756..112831455hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152828
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605498
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