A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6144584



Internal ID9121987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72125525..72126898hg38UCSC Ensembl
Outerchr15:72125488..72126948hg38UCSC Ensembl
Innerchr15:72417866..72419239hg19UCSC Ensembl
Outerchr15:72417829..72419289hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381461
hg191461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675300
Supporting Variants
SamplesNA18523
Known GenesSENP8
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6144584
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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