A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370337



Internal ID21027890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:29656201..29667255hg38UCSC Ensembl
chr4:29657823..29668877hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3811055
hg1911055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115180
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370337
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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