A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157592



Internal ID21460952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107864170..107864489hg38UCSC Ensembl
chr7:107504615..107504934hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5581795
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157592
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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