A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474856



Internal ID22532751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10451028..10452735hg38UCSC Ensembl
chr17:10354345..10356052hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381708
hg191708
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884630
Supporting Variants
Samples
Known GenesMYH4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474856
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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