A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062584



Internal ID21407225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203306072..203306196hg38UCSC Ensembl
chr1:203275200..203275324hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568768
Supporting Variants
SamplesHG00512
Known GenesBTG2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062584
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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