A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378111



Internal ID21035664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70088395..70154980hg38UCSC Ensembl
chr4:70954112..71020697hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3866586
hg1966586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119071
Samples
Known GenesC4orf40, CSN1S2BP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378111
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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