A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320877



Internal ID20853978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:54834901..54840000hg38UCSC Ensembl
chr1:55300574..55305673hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062187
Samples
Known GenesC1orf177
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320877
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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