A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635440



Internal ID7022239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97386032..97386847hg38UCSC Ensembl
Innerchr14:97386044..97386836hg38UCSC Ensembl
Outerchr14:97386021..97386859hg38UCSC Ensembl
chr14:97852369..97853184hg19UCSC Ensembl
Innerchr14:97852381..97853173hg19UCSC Ensembl
Outerchr14:97852358..97853196hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15103710
SamplesNA20894
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635440
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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