A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423127



Internal ID22480997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169555955..169556153hg38UCSC Ensembl
chr6:169956051..169956249hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925577
Supporting Variants
Samples
Known GenesWDR27
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423127
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer