A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316018



Internal ID20849094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37854930..37871768hg38UCSC Ensembl
chr1:38320602..38337440hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3816839
hg1916839
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203056
Samples
Known GenesINPP5B, MTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316018
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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