A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15202500



Internal ID21341305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63674283..63674283hg38UCSC Ensembl
chr6:64384184..64384184hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3936598
Supporting Variants
SamplesHG002
Known GenesPHF3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15202500
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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