A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417861



Internal ID21075414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135151571..135219430hg38UCSC Ensembl
chr7:134836323..134904182hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3867860
hg1967860
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228984
Samples
Known GenesC7orf49, MIR6509, TMEM140, WDR91
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417861
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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