A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13833454



Internal ID3204398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61724899..61725774hg38UCSC Ensembl
Innerchr10:61724917..61725756hg38UCSC Ensembl
Outerchr10:61724881..61725792hg38UCSC Ensembl
chr10:63484657..63485532hg19UCSC Ensembl
Innerchr10:63484675..63485514hg19UCSC Ensembl
Outerchr10:63484639..63485550hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38876
hg19876
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623486
Supporting Variants
SamplesHG02813
Known GenesC10orf107
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13833454
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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