A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349231



Internal ID21006784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216655785..216656539hg38UCSC Ensembl
chr2:217520508..217521262hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38755
hg19755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085785
Samples
Known GenesIGFBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349231
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