A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1336829



Internal ID12153265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49257990..49258366hg38UCSC Ensembl
chr20:47874527..47874903hg19UCSC Ensembl
chr20:47307934..47308310hg18UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38377
hg19377
hg18377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3909104
SamplesHuRef
Known GenesZNFX1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1336829
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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