A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430358



Internal ID21087911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:126563724..126583281hg38UCSC Ensembl
chr7:126203778..126223335hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3819558
hg1919558
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236336
Samples
Known GenesGRM8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430358
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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