A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15192697



Internal ID21331582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47557553..47557553hg38UCSC Ensembl
chr11:47579105..47579105hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38613
hg19613
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3936680
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15192697
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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