A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271704



Internal ID20838744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129758099..137582370hg38UCSC Ensembl
chr7:129397939..137267116hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg387824272
hg197869178
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560945
Supporting Variants
Samples
Known GenesAGBL3, AKR1B1, AKR1B10, AKR1B15, BPGM, C7orf49, C7orf73, CALD1, CEP41, CHCHD3, CHRM2, CNOT4, COPG2, CPA1, CPA2, CPA4, CPA5, DGKI, EXOC4, FAM180A, FLJ40288, KLF14, KLHDC10, LINC-PINT, LOC349160, LOC646329, LRGUK, LUZP6, MEST, MESTIT1, MIR182, MIR183, MIR29A, MIR29B1, MIR335, MIR490, MIR6133, MIR6509, MIR96, MKLN1, MTPN, NUP205, PLXNA4, PODXL, PTN, SLC13A4, SLC35B4, SSMEM1, STRA8, TMEM140, TMEM209, TSGA13, UBE2H, WDR91, ZC3HC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271704
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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