A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504287



Internal ID22562230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99482557..99486425hg38UCSC Ensembl
chr7:99080180..99084048hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg383869
hg193869
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862441
Supporting Variants
Samples
Known GenesZNF789
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504287
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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