A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441680



Internal ID21099233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99317365..100480706hg38UCSC Ensembl
chr10:101077122..102240463hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg381163342
hg191163342
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177693
Samples
Known GenesABCC2, BLOC1S2, CHUK, CNNM1, COX15, CPN1, CUTC, CWF19L1, DNMBP, DNMBP-AS1, ENTPD7, ERLIN1, GOT1, LINC00263, NKX2-3, PKD2L1, SCD, SLC25A28, SNORA12, WNT8B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441680
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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