A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349187



Internal ID21006740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:158167053..158167432hg38UCSC Ensembl
chr2:159023565..159023944hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079838
Samples
Known GenesCCDC148-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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