A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15379394



Internal ID5689945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14535607..14540747hg38UCSC Ensembl
Innerchr16:14535607..14540747hg38UCSC Ensembl
Outerchr16:14535324..14541095hg38UCSC Ensembl
chr16:14629464..14634604hg19UCSC Ensembl
Innerchr16:14629464..14634604hg19UCSC Ensembl
Outerchr16:14629181..14634952hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg385141
hg195141
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638010
Supporting Variants
SamplesNA19085
Known GenesPARN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15379394
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer