A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6340873



Internal ID9318276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:2131551..2131717hg38UCSC Ensembl
Outerchr19:2131394..2131887hg38UCSC Ensembl
Innerchr19:2131550..2131716hg19UCSC Ensembl
Outerchr19:2131393..2131886hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38494
hg19494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2659904
Supporting Variants
SamplesHG00740
Known GenesAP3D1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6340873
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