A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573636



Internal ID21765679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128798330..128798330hg38UCSC Ensembl
chr7:128438384..128438384hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38729
hg19729
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6078973
Supporting Variants
Samples
Known GenesCCDC136
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573636
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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