A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12992390



Internal ID2994206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143728246..143743547hg38UCSC Ensembl
chr7:143425339..143440640hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3815302
hg1915302
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615307
Supporting Variants
SamplesHG01878
Known GenesFAM115C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12992390
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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