A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324952



Internal ID20858082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149957135..149957487hg38UCSC Ensembl
chr1:149929047..149929399hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052933
Samples
Known GenesOTUD7B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324952
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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