A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319975



Internal ID20853072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56967298..57018977hg38UCSC Ensembl
chr1:57432971..57484650hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3851680
hg1951680
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202077
Samples
Known GenesDAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319975
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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