A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427552



Internal ID21085105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148459126..148483045hg38UCSC Ensembl
chr7:148156218..148180137hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3823920
hg1923920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153958
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427552
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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