A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969706



Internal ID18892701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:9786060..9786760hg38UCSC Ensembl
OuterchrX:9754100..9754800hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1122260
Supporting Variants
SamplesKWS2
Known GenesSHROOM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969706
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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