A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17571032



Internal ID21763075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87010163..87010342hg38UCSC Ensembl
chr6:87719881..87720060hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012242
Supporting Variants
Samples
Known GenesHTR1E
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17571032
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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