A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432327



Internal ID21089880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139386464..139390296hg38UCSC Ensembl
chr7:139071210..139075042hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg383833
hg193833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155254
Samples
Known GenesC7orf55-LUC7L2, LUC7L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432327
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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