A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376096



Internal ID21033649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139247027..139271451hg38UCSC Ensembl
chr4:140168181..140192605hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3824425
hg1924425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110174
Samples
Known GenesMGARP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376096
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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