A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1136909



Internal ID11953346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71680692..71680770hg38UCSC Ensembl
chr7:71145677..71145755hg19UCSC Ensembl
chr7:70783613..70783691hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3879
hg1979
hg1879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4078998
SamplesHuRef
Known GenesWBSCR17
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1136909
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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