A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418970



Internal ID21076523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139678761..139687342hg38UCSC Ensembl
chr7:139363507..139372088hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg388582
hg198582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155287
Samples
Known GenesHIPK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418970
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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