A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470631



Internal ID21128184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64935377..65143014hg38UCSC Ensembl
chr11:64702849..64910485hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38207638
hg19207637
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191629
Samples
Known GenesARL2, ARL2-SNX15, BATF2, C11orf85, CDCA5, FAU, GPHA2, MIR6751, MIR6879, MRPL49, NAALADL1, SAC3D1, SNX15, SYVN1, TM7SF2, TMEM262, VPS51, ZFPL1, ZNHIT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470631
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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