A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15499292



Internal ID732820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:64649048..64651410hg38UCSC Ensembl
Innerchr16:64649048..64651410hg38UCSC Ensembl
Outerchr16:64648843..64651568hg38UCSC Ensembl
chr16:64682951..64685313hg19UCSC Ensembl
Innerchr16:64682951..64685313hg19UCSC Ensembl
Outerchr16:64682746..64685471hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg382363
hg192363
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638838
Supporting Variants
SamplesHG00343
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15499292
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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