A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10038877



Internal ID6870798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:103228119..103319499hg38UCSC Ensembl
chr1:103693675..103785057hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3891381
hg1991383
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3587004
Supporting Variants
SamplesNA21097
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10038877
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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