A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17507940



Internal ID22565889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70587422..70595000hg38UCSC Ensembl
chr6:71297125..71304703hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg387579
hg197579
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846066
Supporting Variants
Samples
Known GenesC6orf57
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17507940
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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