A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611955



Internal ID6998857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4897082..4911190hg38UCSC Ensembl
Innerchr7:4897082..4911190hg38UCSC Ensembl
Outerchr7:4896582..4911690hg38UCSC Ensembl
chr7:4936713..4950821hg19UCSC Ensembl
Innerchr7:4936713..4950821hg19UCSC Ensembl
Outerchr7:4936213..4951321hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3814109
hg1914109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12671543, essv12671544
SamplesHG02789, HG01491
Known GenesMMD2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611955
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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