A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419358



Internal ID21076911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:151953680..152196965hg38UCSC Ensembl
chr7:151650765..151894050hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38243286
hg19243286
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7185n223
Supporting Variantsnssv18220136
Samples
Known GenesGALNT11, GALNTL5, KMT2C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419358
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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