A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145213



Internal ID21484109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100254568..100254967hg38UCSC Ensembl
chr7:99852191..99852590hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5583136
Supporting Variants
SamplesNA12329
Known GenesGATS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145213
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