A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619774



Internal ID20992845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44436069..44437040hg38UCSC Ensembl
chr7:44475668..44476639hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38972
hg19972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154603
Samples
Known GenesNUDCD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619774
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