A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340049



Internal ID20997602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:209863172..209867498hg38UCSC Ensembl
chr2:210727896..210732222hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg384327
hg194327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085088
Samples
Known GenesUNC80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340049
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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