A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606524



Internal ID20979595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:123513753..123628513hg38UCSC Ensembl
chr7:123153807..123268567hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38114761
hg19114761
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229057
Samples
Known GenesASB15, IQUB, NDUFA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606524
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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