A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4149122



Internal ID11431660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73711539..73711845hg38UCSC Ensembl
chr6:74421262..74421568hg19UCSC Ensembl
chr6:74477983..74478289hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38307
hg19307
hg18307
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1316113
Supporting Variants
SamplesHuRef
Known GenesCD109
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4149122
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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