A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354949



Internal ID21012502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:158350697..158360892hg38UCSC Ensembl
chr2:159207209..159217404hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3810196
hg1910196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079851
Samples
Known GenesCCDC148
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354949
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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