A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501491



Internal ID22559429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66824885..66836629hg38UCSC Ensembl
chr7:66289872..66301616hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3811745
hg1911745
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852126
Supporting Variants
Samples
Known GenesGTF2IRD1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501491
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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