A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453729



Internal ID22511603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17315495..17316528hg38UCSC Ensembl
chr1:17641990..17643023hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg381034
hg191034
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828547
Supporting Variants
Samples
Known GenesPADI4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453729
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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