A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348855



Internal ID21006408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161973699..161974278hg38UCSC Ensembl
chr2:162830209..162830788hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38580
hg19580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080160
Samples
Known GenesSLC4A10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348855
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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