A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610919



Internal ID20983990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123036318..123133456hg38UCSC Ensembl
chr6:123357463..123454601hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3897139
hg1997139
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214595
Samples
Known GenesCLVS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610919
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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