A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15385603



Internal ID5387419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15407892..15409161hg38UCSC Ensembl
Innerchr16:15407892..15409161hg38UCSC Ensembl
Outerchr16:15407682..15409338hg38UCSC Ensembl
chr16:15501749..15503018hg19UCSC Ensembl
Innerchr16:15501749..15503018hg19UCSC Ensembl
Outerchr16:15501539..15503195hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg381270
hg191270
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638030
Supporting Variants
SamplesNA19028
Known GenesMPV17L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15385603
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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