A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317389



Internal ID20850474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202162007..202169763hg38UCSC Ensembl
chr1:202131135..202138891hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg387757
hg197757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056668
Samples
Known GenesPTPRVP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317389
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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