A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516360



Internal ID15096967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:13839805..13844664hg38UCSC Ensembl
InnerchrX:13857924..13862783hg19UCSC Ensembl
InnerchrX:13767845..13772704hg18UCSC Ensembl
InnerchrX:13617581..13622440hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg384860
hg194860
hg184860
hg174860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv684311, nssv658703, nssv667765
Samples
Known GenesGPM6B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516360
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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