A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327664



Internal ID20860804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:57495222..57499086hg38UCSC Ensembl
chr1:57960894..57964758hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg383865
hg193865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061849
Samples
Known GenesDAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327664
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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