A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150498



Internal ID21460977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:30968640..30968640hg38UCSC Ensembl
chr7:31008255..31008255hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5627321
Supporting Variants
SamplesHG02818
Known GenesGHRHR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150498
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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