A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347097



Internal ID21004650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61119736..61120221hg38UCSC Ensembl
chr2:61346871..61347356hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089455
Samples
Known GenesKIAA1841
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347097
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