A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610112



Internal ID20983183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2407780..2547870hg38UCSC Ensembl
chr7:2447415..2587504hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38140091
hg19140090
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154975
Samples
Known GenesBRAT1, CHST12, LFNG, LOC101927181, MIR4648
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610112
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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