A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17568830



Internal ID21760873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140454278..140454278hg38UCSC Ensembl
chr7:140154078..140154078hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6074575
Supporting Variants
Samples
Known GenesMKRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17568830
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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