A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617607



Internal ID20990678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:140475910..141097571hg38UCSC Ensembl
chr6:140797047..141418708hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38621662
hg19621662
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216890
Samples
Known GenesMIR4465
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617607
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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