A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17507939



Internal ID22565888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70559772..70571763hg38UCSC Ensembl
chr6:71269475..71281466hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3811992
hg1911992
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845355
Supporting Variants
Samples
Known GenesC6orf57, FAM135A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17507939
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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