A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3997620



Internal ID11764253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101925712..101925712hg38UCSC Ensembl
chr11:101796443..101796443hg19UCSC Ensembl
chr11:101301653..101301653hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38826
hg19826
hg18826
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1725395
Supporting Variants
SamplesHuRef
Known GenesKIAA1377
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3997620
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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