A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1584074



Internal ID12747195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:63185573..71722146hg38UCSC Ensembl
chrX:62405045..70941996hg19UCSC Ensembl
chrX:62321770..70858721hg18UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg388536574
hg198536952
hg188536952
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3829597
SamplesHuRef
Known GenesACRC, AMER1, AR, ARHGEF9, ARR3, ASB12, AWAT1, AWAT2, BCYRN1, CXCR3, CXorf49, CXorf49B, CXorf65, DGAT2L6, DLG3, EDA, EDA2R, EFNB1, FAM155B, FOXO4, FRMD8P1, GDPD2, GJB1, HEPH, IGBP1, IL2RG, INGX, ITGB1BP2, KIF4A, LAS1L, LINC00269, LINC00891, LOC100132741, LOC92249, MED12, MIR1468, MIR223, MIR676, MSN, MTMR8, NLGN3, NONO, OGT, OPHN1, OTUD6A, P2RY4, PDZD11, PJA1, RAB41, SLC7A3, SNX12, SPIN4, STARD8, TAF1, TEX11, VSIG4, YIPF6, ZC3H12B, ZC4H2, ZMYM3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1584074
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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