A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332653



Internal ID20865827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:57869669..57871259hg38UCSC Ensembl
chr1:58335341..58336931hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg381591
hg191591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061875
Samples
Known GenesDAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332653
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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