A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329344



Internal ID20862496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:176148501..176149800hg38UCSC Ensembl
chr1:176117637..176118936hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053722
Samples
Known GenesRFWD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329344
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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