A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3505588



Internal ID18803869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46247355..46996235hg19UCSC Ensembl
Innerchr10:45567361..46416241hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg19748881
hg18848881
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036909
Supporting Variants
Samples
Known GenesAGAP4, BMS1P1, BMS1P5, FAM21C, FAM35BP, FRMPD2P1, GLUD1P7, GPRIN2, PTPN20A, PTPN20B, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3505588
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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