A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506807



Internal ID20880093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7472224..7473161hg38UCSC Ensembl
chr17:7375543..7376480hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38938
hg19938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038440
Samples
Known GenesZBTB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506807
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