A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066098



Internal ID21512209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6979792..6979844hg38UCSC Ensembl
chr1:7039852..7039904hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582897
Supporting Variants
SamplesNA24385
Known GenesCAMTA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066098
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