A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990188



Internal ID19236943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:8465459..8467559hg38UCSC Ensembl
OuterchrX:8433500..8435600hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg382101
hg192101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137688
Supporting Variants
SamplesKWS2
Known GenesVCX3B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990188
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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