A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17480767



Internal ID22538671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7585676..7588347hg38UCSC Ensembl
chr1:7645736..7648407hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg382672
hg192672
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830649
Supporting Variants
Samples
Known GenesCAMTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17480767
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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