A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4136080



Internal ID11071933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13063099..13063272hg38UCSC Ensembl
chr10:13105099..13105272hg19UCSC Ensembl
chr10:13145105..13145278hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38174
hg19174
hg18174
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1638252
Supporting Variants
SamplesHuRef
Known GenesCCDC3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4136080
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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