A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639596



Internal ID7026375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89799817..89801341hg38UCSC Ensembl
Innerchr16:89799817..89801341hg38UCSC Ensembl
Outerchr16:89799674..89801447hg38UCSC Ensembl
chr16:89866225..89867749hg19UCSC Ensembl
Innerchr16:89866225..89867749hg19UCSC Ensembl
Outerchr16:89866082..89867855hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381525
hg191525
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15569858, essv15569856, essv15569857, essv15569855, essv15569854
SamplesHG00121, HG03237, HG04158, NA20845, HG02604
Known GenesFANCA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639596
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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