A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17156485



Internal ID21494333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42409727..42409803hg38UCSC Ensembl
chr7:42449326..42449402hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569901
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17156485
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