A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571589



Internal ID20944660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:150466836..151011478hg38UCSC Ensembl
chr7:150163924..150708566hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38544643
hg19544643
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273070
Samples
Known GenesAOC1, GIMAP1, GIMAP1-GIMAP5, GIMAP2, GIMAP4, GIMAP5, GIMAP6, GIMAP7, GIMAP8, KCNH2, NOS3, TMEM176A, TMEM176B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571589
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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