A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319864



Internal ID20852961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235336243..235360708hg38UCSC Ensembl
chr1:235499558..235524023hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3824466
hg1924466
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202418
Samples
Known GenesGGPS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319864
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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