A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509973



Internal ID20883286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63831101..63835800hg38UCSC Ensembl
chr15:64123300..64127999hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193178
Samples
Known GenesHERC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509973
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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