A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613105



Internal ID20986176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27619550..27623737hg38UCSC Ensembl
chr7:27659169..27663356hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg384188
hg194188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157036
Samples
Known GenesHIBADH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613105
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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