A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507203



Internal ID20880491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45736501..45737900hg38UCSC Ensembl
chr17:43813867..43815266hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035921
Samples
Known GenesCRHR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507203
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