A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565144



Internal ID21889499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36732780..36737733hg38UCSC Ensembl
chr6:36700557..36705510hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg384954
hg194954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6011858
Supporting Variants
Samples
Known GenesRAB44
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565144
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