A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1310867



Internal ID12473989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41443195..41443295hg38UCSC Ensembl
chr4:41445212..41445312hg19UCSC Ensembl
chr4:41139969..41140069hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38101
hg19101
hg18101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3624895
SamplesHuRef
Known GenesLIMCH1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1310867
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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