A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341810



Internal ID20999363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102625607..102631279hg38UCSC Ensembl
chr2:103242066..103247738hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg385673
hg195673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075115
Samples
Known GenesSLC9A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341810
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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