A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616704



Internal ID20989775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151822415..151822805hg38UCSC Ensembl
chr6:152143550..152143940hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141518
Samples
Known GenesESR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616704
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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