A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442625



Internal ID21100178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3121305..3126563hg38UCSC Ensembl
chr10:3163497..3168755hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg385259
hg195259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979168
Samples
Known GenesPFKP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442625
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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