A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502625



Internal ID22560566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149088925..149092215hg38UCSC Ensembl
chr7:148786017..148789307hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg383291
hg193291
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854196
Supporting Variants
Samples
Known GenesZNF786
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502625
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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