A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3834



Internal ID15538561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:155346169..155534075hg38UCSC Ensembl
OuterchrX:154575478..154763736hg19UCSC Ensembl
OuterchrX:154228672..154416930hg18UCSC Ensembl
OuterchrX:154139182..154327440hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38187907
hg19188259
hg18188259
hg17188259
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7470
Supporting Variants
SamplesNA12878
Known GenesF8A1, F8A2, F8A3, H2AFB1, H2AFB2, H2AFB3, MIR1184-1, MIR1184-2, MIR1184-3, TMLHE, TMLHE-AS1
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv3834
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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