A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315604



Internal ID20848675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24476201..24481000hg38UCSC Ensembl
chr1:24802691..24807490hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059669
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315604
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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