A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586869



Internal ID6972040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96610434..96656312hg38UCSC Ensembl
Innerchr1:96610434..96656312hg38UCSC Ensembl
Outerchr1:96609934..96656812hg38UCSC Ensembl
chr1:97075990..97121868hg19UCSC Ensembl
Innerchr1:97075990..97121868hg19UCSC Ensembl
Outerchr1:97075490..97122368hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3845879
hg1945879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10025320
SamplesHG02861
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586869
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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