A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15377429



Internal ID846597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12318553..12336324hg38UCSC Ensembl
Innerchr16:12319053..12335824hg38UCSC Ensembl
Outerchr16:12317553..12337324hg38UCSC Ensembl
chr16:12412410..12430181hg19UCSC Ensembl
Innerchr16:12412910..12429681hg19UCSC Ensembl
Outerchr16:12411410..12431181hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3817772
hg1917772
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637958
Supporting Variants
SamplesHG00442
Known GenesSNX29
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15377429
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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