A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1027952



Internal ID11844391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56106814..56106814hg38UCSC Ensembl
chr19:56618183..56618183hg19UCSC Ensembl
chr19:61309995..61309995hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3855
hg1955
hg1855
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4253489
SamplesHuRef
Known GenesZNF787
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1027952
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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