A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454414



Internal ID21111967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26563901..26598200hg38UCSC Ensembl
chr10:26852830..26887129hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3834300
hg1934300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv659n223
Supporting Variantsnssv18194591
Samples
Known GenesAPBB1IP, LINC00264
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454414
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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