A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324991



Internal ID20858121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:175965201..175966200hg38UCSC Ensembl
chr1:175934337..175935336hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053704
Samples
Known GenesRFWD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324991
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