A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355816



Internal ID21013369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4705185..4705686hg38UCSC Ensembl
chr3:4746869..4747370hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100732
Samples
Known GenesITPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355816
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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