A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631704



Internal ID6671829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31751134..31754425hg38UCSC Ensembl
Innerchr13:31751184..31754375hg38UCSC Ensembl
Outerchr13:31751045..31754514hg38UCSC Ensembl
chr13:32325271..32328562hg19UCSC Ensembl
Innerchr13:32325321..32328512hg19UCSC Ensembl
Outerchr13:32325182..32328651hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg383292
hg193292
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14683610, essv14683609, essv14683608
SamplesHG02658, HG00272, HG00182
Known GenesRXFP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631704
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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