A curated catalogue of human genomic structural variation




Variant Details

Variant: esv987977



Internal ID7060277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35772678..35772678hg38UCSC Ensembl
chr4:35774300..35774300hg19UCSC Ensembl
chr4:35450695..35450695hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38138
hg19138
hg18138
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3573936
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv987977
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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