A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319931



Internal ID20853028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:175436834..175442446hg38UCSC Ensembl
chr1:175405970..175411582hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg385613
hg195613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054365
Samples
Known GenesTNR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319931
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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