A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15060887



Internal ID1938268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73912237..73914241hg38UCSC Ensembl
Innerchr14:73912296..73914183hg38UCSC Ensembl
Outerchr14:73912179..73914300hg38UCSC Ensembl
chr14:74378940..74380944hg19UCSC Ensembl
Innerchr14:74378999..74380886hg19UCSC Ensembl
Outerchr14:74378882..74381003hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382005
hg192005
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634923
Supporting Variants
SamplesHG01804
Known GenesZNF410
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15060887
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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