A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15201541



Internal ID21340340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96896864..96896864hg38UCSC Ensembl
chr5:96232568..96232568hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3951202
Supporting Variants
SamplesHG002
Known GenesERAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15201541
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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