A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614608



Internal ID20987679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43757901..43759400hg38UCSC Ensembl
chr7:43797500..43798999hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219709
Samples
Known GenesBLVRA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614608
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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