A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320906



Internal ID20854007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44741125..44741731hg38UCSC Ensembl
chr1:45206797..45207403hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061411
Samples
Known GenesKIF2C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320906
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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