A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316711



Internal ID20849792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6258028..6295606hg38UCSC Ensembl
chr1:6318088..6355666hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3837579
hg1937579
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203662
Samples
Known GenesACOT7, GPR153
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316711
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer