A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500029



Internal ID22557965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:982499..1004947hg38UCSC Ensembl
chr6:982736..1005182hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3822449
hg1922447
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846387
Supporting Variants
Samples
Known GenesLOC285768
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500029
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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