A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436961



Internal ID21094514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45179801..45181600hg38UCSC Ensembl
chr10:45675249..45677048hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192817
Samples
Known GenesANKRD30BP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436961
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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