A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1739869



Internal ID12556301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24345073..24345073hg38UCSC Ensembl
chr1:24671563..24671563hg19UCSC Ensembl
chr1:24544150..24544150hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38315
hg19315
hg18315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4074743
SamplesHuRef
Known GenesGRHL3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1739869
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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