A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4271472



Internal ID11207324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36363416..36363416hg38UCSC Ensembl
chr6:36331193..36331193hg19UCSC Ensembl
chr6:36439171..36439171hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38102
hg19102
hg18102
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1651866
Supporting Variants
SamplesHuRef
Known GenesETV7
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4271472
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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