A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969702



Internal ID19231260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:1637107..1639407hg38UCSC Ensembl
OuterchrX:1756000..1758300hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg382301
hg192301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1122258
Supporting Variants
SamplesKWS2
Known GenesASMT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969702
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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