A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549568



Internal ID20922729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:246578459..247400067hg38UCSC Ensembl
chr1:246741761..247563369hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38821609
hg19821609
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251478
Samples
Known GenesAHCTF1, C1orf229, CNST, LOC149134, MIR3916, SCCPDH, VN1R5, ZNF124, ZNF496, ZNF669, ZNF670, ZNF670-ZNF695, ZNF695
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549568
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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