A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672879



Internal ID9592298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84183868..85188485hg38UCSC Ensembl
Outerchr15:84183834..85188520hg38UCSC Ensembl
Innerchr15:84852620..85731716hg19UCSC Ensembl
Outerchr15:84852586..85731751hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg381004687
hg19879166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5935433, essv6354851
SamplesNA19390, HG01383
Known GenesALPK3, DNM1P41, GOLGA6L4, GOLGA6L5P, LINC00933, LOC388152, LOC440300, LOC642423, NMB, PDE8A, SCAND2P, SEC11A, SLC28A1, UBE2Q2P1, WDR73, ZNF592, ZSCAN2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672879
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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