A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17508029



Internal ID22565978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:77552988..77567167hg38UCSC Ensembl
chr6:78262705..78276884hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3814180
hg1914180
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845449
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17508029
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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