A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067222



Internal ID21502894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7337595..7337595hg38UCSC Ensembl
chr1:7397655..7397655hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608272
Supporting Variants
SamplesNA19239
Known GenesCAMTA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067222
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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