A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504638



Internal ID22562581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154612559..154614158hg38UCSC Ensembl
chr7:154404269..154405868hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855168
Supporting Variants
Samples
Known GenesDPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504638
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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