A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6764897



Internal ID10001360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:1408506..1410306hg38UCSC Ensembl
OuterchrX:1527399..1529199hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg381801
hg191801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739692, esv2739688, esv2739704, esv2739690, esv2739686
Supporting Variants
SamplesSSM008
Known GenesASMTL, ASMTL-AS1
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)essv6764897
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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