A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13770723



Internal ID3750037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45596912..45624974hg38UCSC Ensembl
Innerchr10:45596912..45624974hg38UCSC Ensembl
Outerchr10:45596412..45625474hg38UCSC Ensembl
chr10:46092360..46120422hg19UCSC Ensembl
Innerchr10:46092360..46120422hg19UCSC Ensembl
Outerchr10:46091860..46120922hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3828063
hg1928063
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623100
Supporting Variants
SamplesHG03380
Known GenesZFAND4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13770723
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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