A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481220



Internal ID22539124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7616523..7620672hg38UCSC Ensembl
chr1:7676583..7680732hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg384150
hg194150
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830149
Supporting Variants
Samples
Known GenesCAMTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481220
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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