A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275587



Internal ID20842627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:34818072..37653201hg38UCSC Ensembl
chr7:34857684..37692804hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg382835130
hg192835121
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559554
Supporting Variants
Samples
Known GenesANLN, AOAH, AOAH-IT1, DPY19L1, DPY19L2P1, EEPD1, ELMO1, ELMO1-AS1, HERPUD2, KIAA0895, LOC100506725, LOC101928618, LOC401324, MIR1200, NPSR1, NPSR1-AS1, SEPT7, TBX20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275587
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0011


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