A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9890089



Internal ID2960502
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585494
Supporting Variants
SamplesHG02614
Known GenesCNR2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9890089
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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