A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461324



Internal ID21118877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:85156741..85385498hg38UCSC Ensembl
chr12:85550519..85779276hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38228758
hg19228758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004249
Samples
Known GenesALX1, LRRIQ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461324
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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