A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1406872



Internal ID12569994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2377745..2378251hg38UCSC Ensembl
chr7:2417380..2417886hg19UCSC Ensembl
chr7:2383906..2384412hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38507
hg19507
hg18507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4265574
SamplesHuRef
Known GenesEIF3B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1406872
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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