A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3707691



Internal ID18659286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14711571..14869583hg38UCSC Ensembl
Innerchr10:14753570..14911582hg19UCSC Ensembl
Innerchr10:14793576..14951588hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38158013
hg19158013
hg18158013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043133
Supporting Variants
Samples
Known GenesCDNF, FAM107B, HSPA14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3707691
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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