A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3584977



Internal ID6972501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:777664..820586hg38UCSC Ensembl
chr1:713044..755966hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3842923
hg1942923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9839038, essv9839039, essv9839037
SamplesNA18976, HG01444, NA20520
Known GenesFAM87B, LOC100288069
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3584977
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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