A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607048



Internal ID20980119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35095401..35103800hg38UCSC Ensembl
chr7:35135013..35143412hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg388400
hg198400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153101
Samples
Known GenesDPY19L2P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607048
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