A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1193325



Internal ID12356448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2773783..2773783hg38UCSC Ensembl
chr6:2774017..2774017hg19UCSC Ensembl
chr6:2719016..2719016hg18UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38294
hg19294
hg18294
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3853971
SamplesHuRef
Known GenesWRNIP1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1193325
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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