A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331526



Internal ID20864690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154947101..154948800hg38UCSC Ensembl
chr1:154919577..154921276hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052051
Samples
Known GenesPBXIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331526
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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