A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317488



Internal ID20850574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39394295..39408784hg38UCSC Ensembl
chr1:39859967..39874456hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3814490
hg1914490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060107
Samples
Known GenesMACF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317488
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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