A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17647863



Internal ID21839910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52433330..55652521hg38UCSC Ensembl
chrX:52176473..55678954hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg383219192
hg193502482
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107207
Supporting Variants
Samples
Known GenesALAS2, APEX2, FAM104B, FAM120C, FAM156A, FAM156B, FGD1, FOXR2, GNL3L, GPR173, HSD17B10, HUWE1, IQSEC2, ITIH6, KDM5C, MAGED2, MAGEH1, MIR4536-1, MIR6857, MIR6894, MIR6895, MIR98, MIRLET7F2, MTRNR2L10, PAGE2, PAGE2B, PAGE3, PAGE5, PFKFB1, PHF8, RIBC1, SMC1A, SNORA11, SPANXN5, SSX2, SSX2B, SSX7, SSX8, TRO, TSPYL2, TSR2, USP51, WNK3, XAGE1A, XAGE1B, XAGE1C, XAGE1D, XAGE1E, XAGE2, XAGE2B, XAGE3, XAGE5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17647863
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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