A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335671



Internal ID20993224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215382213..215733533hg38UCSC Ensembl
chr2:216246936..216598256hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38351321
hg19351321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084033
Samples
Known GenesFN1, LINC00607
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335671
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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