A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155235



Internal ID21425578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:782117..782117hg38UCSC Ensembl
chr7:821754..821754hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632140
Supporting Variants
SamplesHG00731
Known GenesHEATR2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155235
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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