A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334662



Internal ID20867849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41197285..41197935hg38UCSC Ensembl
chr1:41662957..41663607hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060796
Samples
Known GenesSCMH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334662
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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