A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155588



Internal ID21408050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90290743..90290792hg38UCSC Ensembl
chr7:89920057..89920106hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570438
Supporting Variants
SamplesHG00512
Known GenesC7orf63
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155588
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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