A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329149



Internal ID20862300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10006969..10008630hg38UCSC Ensembl
chr1:10067027..10068688hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381662
hg191662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049563
Samples
Known GenesRBP7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329149
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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