A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504269



Internal ID22562212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98199717..98216759hg38UCSC Ensembl
chr7:97829029..97846071hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3817043
hg1917043
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863788
Supporting Variants
Samples
Known GenesBHLHA15, LMTK2, TECPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504269
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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