A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320855



Internal ID20853956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173126001..173129200hg38UCSC Ensembl
chr1:173095140..173098339hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053972
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320855
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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