A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612241



Internal ID20985312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102751801..102754000hg38UCSC Ensembl
chr7:102392248..102394447hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151289
Samples
Known GenesFAM185A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612241
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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