A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335195



Internal ID20868387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244853689..244854307hg38UCSC Ensembl
chr1:245016991..245017609hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38619
hg19619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059678
Samples
Known GenesHNRNPU
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335195
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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