A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437992



Internal ID22495862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95405761..95405852hg38UCSC Ensembl
chr7:95035073..95035164hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5919706
Supporting Variants
Samples
Known GenesPON2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437992
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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