A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3992587



Internal ID19243922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:101432911..101432961hg38UCSC Ensembl
OuterchrX:100687899..100687949hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1141073
Supporting Variants
SamplesKWS2
Known GenesARMCX4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3992587
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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