A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5608810



Internal ID21557115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156928416..156928416hg38UCSC Ensembl
chr1:156898208..156898208hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061194
SamplesHG02011
Known GenesLRRC71
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5608810
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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