A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437560



Internal ID21095113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73673561..73872094hg38UCSC Ensembl
chr10:75433319..75631852hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38198534
hg19198534
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195382
Samples
Known GenesAGAP5, BMS1P4, CAMK2G, CHCHD1, FUT11, GLUD1P3, NDST2, SEC24C, ZSWIM8, ZSWIM8-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437560
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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