A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17507949



Internal ID22565898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71418981..71422138hg38UCSC Ensembl
chr6:72128684..72131841hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg383158
hg193158
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845361
Supporting Variants
Samples
Known GenesLINC00472
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17507949
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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