A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15329462



Internal ID6110631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96270178..96271653hg38UCSC Ensembl
Innerchr15:96270178..96271653hg38UCSC Ensembl
Outerchr15:96270002..96271834hg38UCSC Ensembl
chr15:96813407..96814882hg19UCSC Ensembl
Innerchr15:96813407..96814882hg19UCSC Ensembl
Outerchr15:96813231..96815063hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg381476
hg191476
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637351
Supporting Variants
SamplesNA19651
Known GenesNR2F2-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15329462
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