A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326700



Internal ID20859837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19979683..19986223hg38UCSC Ensembl
chr1:20306176..20312716hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg386541
hg196541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056571
Samples
Known GenesPLA2G2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326700
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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