A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500781



Internal ID22558718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:120217471..120221696hg38UCSC Ensembl
chr7:119857525..119861750hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg384226
hg194226
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860185
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500781
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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