A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6778696



Internal ID10184308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:1424990..1425163hg38UCSC Ensembl
OuterchrX:1543883..1544056hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739692, esv2739709, esv2739688, esv2739690, esv2739686
Supporting Variants
SamplesSSM067
Known GenesASMTL
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)essv6778696
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer