A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433768



Internal ID22491638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:34818028..37653165hg38UCSC Ensembl
chr7:34857640..37692768hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg382835138
hg192835129
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975022
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
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433768
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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