A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936820



Internal ID21356889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75595250..75595250hg38UCSC Ensembl
chr7:75224568..75224568hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15203644
SamplesHG002
Known GenesHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936820
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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