A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15398501



Internal ID1464172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19125517..19174532hg38UCSC Ensembl
Innerchr16:19125667..19174382hg38UCSC Ensembl
Outerchr16:19125367..19174682hg38UCSC Ensembl
chr16:19136839..19185854hg19UCSC Ensembl
Innerchr16:19136989..19185704hg19UCSC Ensembl
Outerchr16:19136689..19186004hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3849016
hg1949016
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638120
Supporting Variants
SamplesHG01353
Known GenesSYT17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15398501
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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