A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4269737



Internal ID11205589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1701183..1701605hg38UCSC Ensembl
chr10:1743377..1743799hg19UCSC Ensembl
chr10:1733377..1733799hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38423
hg19423
hg18423
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1631254
Supporting Variants
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4269737
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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