A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607323



Internal ID20980394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149759123..149759743hg38UCSC Ensembl
chr6:150080259..150080879hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141891
Samples
Known GenesPCMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607323
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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