A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936071



Internal ID21356140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206524558..206524558hg38UCSC Ensembl
chr1:206697891..206697891hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189181
SamplesHG002
Known GenesRASSF5
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936071
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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