A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611186



Internal ID20984257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27136039..27383176hg38UCSC Ensembl
chr7:27175658..27422795hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38247138
hg19247138
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218739
Samples
Known GenesEVX1, HOTTIP, HOXA10, HOXA10-HOXA9, HOXA11, HOXA11-AS, HOXA13, HOXA5, HOXA6, HOXA7, HOXA9, HOXA-AS3, HOXA-AS4, MIR196B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611186
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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