A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318920



Internal ID20852012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7971825..7988548hg38UCSC Ensembl
chr1:8031885..8048608hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3816724
hg1916724
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204485
Samples
Known GenesPARK7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318920
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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