A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643396



Internal ID6683474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1356856..1396468hg38UCSC Ensembl
chr19:1356855..1396467hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3839613
hg1939613
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15968113, essv15968115, essv15968114
SamplesHG02318, NA19020, HG00867
Known GenesMUM1, NDUFS7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643396
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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