A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509632



Internal ID22567582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128290816..128307872hg38UCSC Ensembl
chr7:127930869..127947925hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3817057
hg1917057
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865466
Supporting Variants
Samples
Known GenesMGC27345
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509632
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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