A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202457



Internal ID20769497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37507754..37544375hg38UCSC Ensembl
chr1:37973355..38009976hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3836622
hg1936622
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331866
Supporting Variants
Samples
Known GenesMEAF6, SNIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202457
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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