A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321039



Internal ID20854141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:176144950..176145505hg38UCSC Ensembl
chr1:176114086..176114641hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053721
Samples
Known GenesRFWD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321039
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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