A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352248



Internal ID22577917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76934641..76934778hg38UCSC Ensembl
chr10:78694399..78694536hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5919447
Supporting Variants
Samples
Known GenesKCNMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352248
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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