A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509306



Internal ID22567256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74662645..74665444hg38UCSC Ensembl
chr7:74076977..74079776hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853583
Supporting Variants
Samples
Known GenesGTF2I
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509306
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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