A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321212



Internal ID20854315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37927739..37939645hg38UCSC Ensembl
chr1:38393411..38405317hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3811907
hg1911907
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203057
Samples
Known GenesINPP5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321212
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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