A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318387



Internal ID20851479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202865602..202868366hg38UCSC Ensembl
chr1:202834730..202837494hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382765
hg192765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056703
Samples
Known GenesLOC148709
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318387
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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