A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612887



Internal ID6999786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38614276..38616235hg38UCSC Ensembl
Innerchr7:38614301..38616211hg38UCSC Ensembl
Outerchr7:38614252..38616260hg38UCSC Ensembl
chr7:38653876..38655835hg19UCSC Ensembl
Innerchr7:38653901..38655811hg19UCSC Ensembl
Outerchr7:38653852..38655860hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381960
hg191960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12744604, essv12744605
SamplesHG01986, HG01889
Known GenesAMPH
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612887
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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