A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152992



Internal ID21443293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76265824..76266167hg38UCSC Ensembl
chr7:75895142..75895485hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571157
Supporting Variants
SamplesHG00732
Known GenesSRRM3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152992
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