A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317119



Internal ID20850203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:861828..1087228hg38UCSC Ensembl
chr1:797208..1022608hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38225401
hg19225401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205176
Samples
Known GenesAGRN, C1orf159, C1orf170, FAM41C, HES4, ISG15, KLHL17, LOC100130417, NOC2L, PLEKHN1, RNF223, SAMD11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317119
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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