A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460737



Internal ID22518620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:52473286..52491754hg38UCSC Ensembl
chr12:52867070..52885538hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3818469
hg1918469
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849874
Supporting Variants
Samples
Known GenesKRT6A, KRT6C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460737
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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