A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17507298



Internal ID22565246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:65758165..65786305hg38UCSC Ensembl
chr6:66468058..66496198hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3828141
hg1928141
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845927
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17507298
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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