A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4305362



Internal ID11241214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29729684..29729684hg38UCSC Ensembl
chr10:30018613..30018613hg19UCSC Ensembl
chr10:30058619..30058619hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38174
hg19174
hg18174
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1019439
Supporting Variants
SamplesHuRef
Known GenesSVIL
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4305362
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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