A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585494



Internal ID6973017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23889782..23890720hg38UCSC Ensembl
Innerchr1:23889791..23890711hg38UCSC Ensembl
Outerchr1:23889773..23890729hg38UCSC Ensembl
chr1:24216272..24217210hg19UCSC Ensembl
Innerchr1:24216281..24217201hg19UCSC Ensembl
Outerchr1:24216263..24217219hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38939
hg19939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9890088, essv9890089
SamplesHG02614, HG02610
Known GenesCNR2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585494
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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