A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009050



Internal ID19098268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16709707..16785052hg38UCSC Ensembl
Innerchr1:17036202..17111547hg19UCSC Ensembl
Innerchr1:16908789..16984134hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3875346
hg1975346
hg1875346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3482504
Samples
Known GenesESPNP, LOC729574, MST1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009050
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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