A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6170700



Internal ID9148103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13014294..13019078hg38UCSC Ensembl
chr10:13056294..13061078hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg384785
hg194785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661464
Supporting Variants
SamplesHG00158
Known GenesCCDC3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6170700
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