A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv675078



Internal ID15411730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46990728..47650490hg19UCSC Ensembl
Innerchr10:46410734..47120496hg18UCSC Ensembl
Innerchr10:46410734..47120496hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19659763
hg18709763
hg17709763
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516485
Supporting Variants
Samples
Known GenesAGAP9, ANTXRLP1, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, FAM35DP, GPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv675078
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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