A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438049



Internal ID21095602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22678116..22684826hg38UCSC Ensembl
chr10:22967045..22973755hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg386711
hg196711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979684
Samples
Known GenesPIP4K2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438049
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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