A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17507964



Internal ID22565913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73165115..73166621hg38UCSC Ensembl
chr6:73874838..73876344hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg381507
hg191507
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845956
Supporting Variants
Samples
Known GenesKCNQ5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17507964
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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