A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1583704



Internal ID12400139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59681429..59681663hg38UCSC Ensembl
chr10:61441187..61441421hg19UCSC Ensembl
chr10:61111193..61111427hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38235
hg19235
hg18235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4325357
SamplesHuRef
Known GenesSLC16A9
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1583704
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer