A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13894414



Internal ID4324181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91363140..91366507hg38UCSC Ensembl
Innerchr10:91363173..91366474hg38UCSC Ensembl
Outerchr10:91363107..91366540hg38UCSC Ensembl
chr10:93122897..93126264hg19UCSC Ensembl
Innerchr10:93122930..93126231hg19UCSC Ensembl
Outerchr10:93122864..93126297hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg383368
hg193368
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624206
Supporting Variants
SamplesHG03870
Known GenesLOC100188947
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13894414
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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