A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999485



Internal ID17292437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:73985566..73987665hg38UCSC Ensembl
OuterchrX:73205401..73207500hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953431
Supporting Variants
SamplesBILGI_BIOE
Known GenesJPX
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999485
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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