A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507182



Internal ID20880470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41369559..41382000hg38UCSC Ensembl
chr17:39525811..39538252hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3812442
hg1912442
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192104
Samples
Known GenesKRT33B, KRT34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507182
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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