A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316412



Internal ID20849491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:95938013..95945092hg38UCSC Ensembl
chr1:96403569..96410648hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg387080
hg197080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065269
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316412
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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