A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13863625



Internal ID3865441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74564188..74567585hg38UCSC Ensembl
chr10:76323946..76327343hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg383398
hg193398
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623831
Supporting Variants
SamplesHG01628
Known GenesADK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13863625
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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