A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17158206



Internal ID21455162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108163968..108164150hg38UCSC Ensembl
chr7:107804413..107804595hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5576806
Supporting Variants
SamplesHG02011
Known GenesNRCAM
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17158206
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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