A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124492



Internal ID19263598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:5652295..5652639hg38UCSC Ensembl
OuterchrX:5570336..5570680hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3975787, nssv3960426
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124492
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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