A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335250



Internal ID20868442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44741162..44742569hg38UCSC Ensembl
chr1:45206834..45208241hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg381408
hg191408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061412
Samples
Known GenesKIF2C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335250
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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