A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612505



Internal ID6652719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21462186..21465457hg38UCSC Ensembl
Innerchr7:21462186..21465457hg38UCSC Ensembl
Outerchr7:21461909..21465713hg38UCSC Ensembl
chr7:21501804..21505075hg19UCSC Ensembl
Innerchr7:21501804..21505075hg19UCSC Ensembl
Outerchr7:21501527..21505331hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg383272
hg193272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12693845, essv12693846, essv12693844, essv12693843
SamplesHG02562, HG02568, NA19321, HG02768
Known GenesSP4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612505
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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