A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317401



Internal ID20850486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:98662338..98668660hg38UCSC Ensembl
chr1:99127894..99134216hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg386323
hg196323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065916
Samples
Known GenesSNX7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317401
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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