A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613146



Internal ID20986217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116966533..116975607hg38UCSC Ensembl
chr7:116606587..116615661hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg389075
hg199075
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148609
Samples
Known GenesST7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613146
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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