A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3508574



Internal ID18460169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46332711..46606240hg38UCSC Ensembl
Innerchr10:46943377..47249575hg19UCSC Ensembl
Innerchr10:46363383..46669581hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38273530
hg19306199
hg18306199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039576
Supporting Variants
Samples
Known GenesAGAP9, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, GPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3508574
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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