A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15187529



Internal ID21326362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165708137..165708137hg38UCSC Ensembl
chr1:165677374..165677374hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3945758
Supporting Variants
SamplesHG002
Known GenesLOC440700
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15187529
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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