A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347905



Internal ID21005458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:185574661..186006700hg38UCSC Ensembl
chr2:186439388..186871427hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38432040
hg19432040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083128
Samples
Known GenesFSIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347905
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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