A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321177



Internal ID20854280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17315532..17316425hg38UCSC Ensembl
chr1:17642027..17642920hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38894
hg19894
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053974
Samples
Known GenesPADI4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321177
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