A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15203126



Internal ID21341936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100172697..100172697hg38UCSC Ensembl
chr7:99770320..99770320hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3939493
Supporting Variants
SamplesHG002
Known GenesGPC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15203126
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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