A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375401



Internal ID22601070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8481076..8481144hg38UCSC Ensembl
chr17:8384394..8384462hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943714
Supporting Variants
Samples
Known GenesMYH10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375401
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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