A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431002



Internal ID22488872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95780028..95780395hg38UCSC Ensembl
chr6:96227904..96228271hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901278
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431002
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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