A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15357238



Internal ID3758870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:921297..922718hg38UCSC Ensembl
Innerchr16:921326..922690hg38UCSC Ensembl
Outerchr16:921269..922747hg38UCSC Ensembl
chr16:971297..972718hg19UCSC Ensembl
Innerchr16:971326..972690hg19UCSC Ensembl
Outerchr16:971269..972747hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381422
hg191422
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637598
Supporting Variants
SamplesHG03388
Known GenesLMF1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15357238
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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