A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023950



Internal ID19113167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:37688820..37700592hg38UCSC Ensembl
Innerchr9:37688817..37700589hg19UCSC Ensembl
Innerchr9:37678817..37690589hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3811773
hg1911773
hg1811773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688889
Samples
Known GenesFRMPD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023950
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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