A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3829597



Internal ID11585588
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 StatusS
Merged Variantsesv1584074
Supporting Variants
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)essv3829597
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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