A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435638



Internal ID22493508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97217802..97217802hg38UCSC Ensembl
chr7:96847114..96847114hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5964145
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435638
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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