A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643395



Internal ID6683473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1356856..1396468hg38UCSC Ensembl
chr19:1356855..1396467hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3839613
hg1939613
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15968112
SamplesHG00266
Known GenesMUM1, NDUFS7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643395
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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