A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316697



Internal ID20849778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93103396..93103686hg38UCSC Ensembl
chr1:93568953..93569243hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065223
Samples
Known GenesMTF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316697
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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