A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6469451



Internal ID9446854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93648980..93650038hg38UCSC Ensembl
chr5:92984686..92985744hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg381059
hg191059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2664180
Supporting Variants
SamplesNA19391
Known GenesFAM172A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6469451
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