A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4266438



Internal ID11548976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75683924..75683983hg38UCSC Ensembl
chr7:75313242..75313301hg19UCSC Ensembl
chr7:75151178..75151237hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3860
hg1960
hg1860
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1647869
Supporting Variants
SamplesHuRef
Known GenesHIP1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4266438
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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