A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502253



Internal ID22560193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165467709..165468708hg38UCSC Ensembl
chr6:165881197..165882196hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844189
Supporting Variants
Samples
Known GenesPDE10A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502253
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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