A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377001



Internal ID21034554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139632432..139639653hg38UCSC Ensembl
chr4:140553586..140560807hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg387222
hg197222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108058
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377001
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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