A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15385528



Internal ID1583562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15031773..15047500hg38UCSC Ensembl
chr16:15125630..15141357hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3815728
hg1915728
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638022
Supporting Variants
SamplesHG01464
Known GenesNTAN1, PDXDC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15385528
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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