A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424142



Internal ID21081695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157501643..157535516hg38UCSC Ensembl
chr7:157294337..157328210hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3833874
hg1933874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151533
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424142
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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