A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316645



Internal ID20849726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41051229..41062751hg38UCSC Ensembl
chr1:41516901..41528423hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3811523
hg1911523
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203112
Samples
Known GenesSCMH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316645
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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