A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17156612



Internal ID21452621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75600639..75601295hg38UCSC Ensembl
chr7:75229957..75230613hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38657
hg19657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568097
Supporting Variants
SamplesHG01596
Known GenesHIP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17156612
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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