A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6215963



Internal ID9689408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93433607..93437994hg38UCSC Ensembl
Outerchr9:93433570..93438044hg38UCSC Ensembl
Innerchr9:96195889..96200276hg19UCSC Ensembl
Outerchr9:96195852..96200326hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg384475
hg194475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2660356
Supporting Variants
SamplesNA19439
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6215963
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