A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319677



Internal ID20852772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1923928..2007755hg38UCSC Ensembl
chr1:1855367..1939194hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3883828
hg1983828
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199836
Samples
Known GenesKIAA1751
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319677
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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