A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321156



Internal ID20854259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150117317..150119850hg38UCSC Ensembl
chr1:150089435..150091968hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg382534
hg192534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052943
Samples
Known GenesVPS45
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321156
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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