A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516695



Internal ID20890056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:2984988..2985362hg38UCSC Ensembl
chr18:2984986..2985360hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039633
Samples
Known GenesLPIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516695
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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