A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331484



Internal ID20864647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:57112394..57112826hg38UCSC Ensembl
chr1:57578067..57578499hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38433
hg19433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062390
Samples
Known GenesDAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331484
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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