A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387695



Internal ID21045248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109711757..109715288hg38UCSC Ensembl
chr4:110632913..110636444hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg383532
hg193532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107768
Samples
Known GenesPLA2G12A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387695
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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