A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499898



Internal ID20873123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79273001..79324700hg38UCSC Ensembl
chr15:79565343..79617042hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3851700
hg1951700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186229
Samples
Known GenesANKRD34C, LOC729911, TMED3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499898
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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