A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472495



Internal ID21130048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71600178..71900170hg38UCSC Ensembl
chr11:71311224..71611216hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38299993
hg19299993
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195457
Samples
Known GenesALG1L9P, DEFB108B, FAM86C1, LOC100129216, LOC100133315, ZNF705E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472495
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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