A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15201875



Internal ID21340680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2504884..2504884hg38UCSC Ensembl
chr6:2505118..2505118hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38432
hg19432
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3934708
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15201875
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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