A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1157499



Internal ID11973936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137199538..137199538hg38UCSC Ensembl
chr6:137520675..137520675hg19UCSC Ensembl
chr6:137562368..137562368hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38133
hg19133
hg18133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3963323
SamplesHuRef
Known GenesIFNGR1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1157499
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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