A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610974



Internal ID20984045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:112695601..112703100hg38UCSC Ensembl
chr7:112335656..112343155hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7087n223
Supporting Variantsnssv18222272
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610974
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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