A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622830



Internal ID7009688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32468577..32479193hg38UCSC Ensembl
Innerchr10:32468577..32479193hg38UCSC Ensembl
Outerchr10:32468077..32479693hg38UCSC Ensembl
chr10:32757505..32768121hg19UCSC Ensembl
Innerchr10:32757505..32768121hg19UCSC Ensembl
Outerchr10:32757005..32768621hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3810617
hg1910617
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13750218
SamplesHG02312
Known GenesCCDC7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622830
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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