A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15359751



Internal ID5361567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1356674..1364974hg38UCSC Ensembl
Innerchr16:1356674..1364974hg38UCSC Ensembl
Outerchr16:1356617..1365011hg38UCSC Ensembl
chr16:1406675..1414975hg19UCSC Ensembl
Innerchr16:1406675..1414975hg19UCSC Ensembl
Outerchr16:1406618..1415012hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg388301
hg198301
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637614
Supporting Variants
SamplesHG03517
Known GenesGNPTG, UNKL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15359751
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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