A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674315



Internal ID9593734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:75000087..75002577hg38UCSC Ensembl
Outerchr10:74999930..75002730hg38UCSC Ensembl
Innerchr10:76759845..76762335hg19UCSC Ensembl
Outerchr10:76759688..76762488hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg382801
hg192801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6493409, essv6240614
SamplesNA19395, NA19189
Known GenesKAT6B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674315
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