A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318503



Internal ID20851595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52178287..52198966hg38UCSC Ensembl
chr1:52643959..52664638hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3820680
hg1920680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061448
Samples
Known GenesZFYVE9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318503
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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