A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585032



Internal ID6625350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2776470..2780643hg38UCSC Ensembl
Innerchr1:2776470..2780643hg38UCSC Ensembl
Outerchr1:2776299..2780800hg38UCSC Ensembl
chr1:2693016..2697186hg19UCSC Ensembl
Innerchr1:2693016..2697186hg19UCSC Ensembl
Outerchr1:2692845..2697343hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg384174
hg194171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9841900
SamplesHG00404
Known GenesTTC34
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585032
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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