A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501312



Internal ID22559250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134629044..134639243hg38UCSC Ensembl
chr7:134313796..134323995hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3810200
hg1910200
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861034
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501312
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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