A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493465



Internal ID22551394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:30755967..30760374hg38UCSC Ensembl
chr4:30757589..30761996hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg384408
hg194408
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838980
Supporting Variants
Samples
Known GenesPCDH7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493465
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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