A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13904636



Internal ID5518096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95447287..95448483hg38UCSC Ensembl
Innerchr10:95447287..95448483hg38UCSC Ensembl
Outerchr10:95447089..95448734hg38UCSC Ensembl
chr10:97207044..97208240hg19UCSC Ensembl
Innerchr10:97207044..97208240hg19UCSC Ensembl
Outerchr10:97206846..97208491hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg381197
hg191197
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624278
Supporting Variants
SamplesNA18991
Known GenesSORBS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13904636
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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