A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978371



Internal ID19226292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:68736558..68748158hg38UCSC Ensembl
OuterchrX:67956400..67968000hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3811601
hg1911601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140035
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978371
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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