A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4156256



Internal ID11092108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91797444..91797743hg38UCSC Ensembl
chr9:94559726..94560025hg19UCSC Ensembl
chr9:93599547..93599846hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1763164
Supporting Variants
SamplesHuRef
Known GenesROR2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4156256
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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