A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519485



Internal ID15100092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:155507715..155699751hg38UCSC Ensembl
InnerchrX:154737376..154929412hg19UCSC Ensembl
InnerchrX:154390570..154582606hg18UCSC Ensembl
InnerchrX:154301080..154493116hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38192037
hg19192037
hg18192037
hg17192037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696877
Samples
Known GenesTMLHE
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519485
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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