A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556652



Internal ID20929723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32865301..34895818hg38UCSC Ensembl
chr7:32904913..34935430hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg382030518
hg192030518
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275554
Samples
Known GenesBBS9, BMPER, FKBP9, KBTBD2, NPSR1, NPSR1-AS1, NT5C3A, RP9, RP9P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556652
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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