A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977882



Internal ID19228672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:2749459..2763259hg38UCSC Ensembl
OuterchrX:2667500..2681300hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3813801
hg1913801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125076
Supporting Variants
SamplesKWS2
Known GenesXG, XGPY2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977882
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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