A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073448



Internal ID21982681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:96661002..96661002hg38UCSC Ensembl
chr7:96290314..96290314hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576673
Samples
Known GenesLOC100506136
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073448
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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