A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013849



Internal ID19103068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:97086260..97545714hg38UCSC Ensembl
Innerchr2:97751997..98162177hg19UCSC Ensembl
Innerchr2:97115724..97528609hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38459455
hg19410181
hg18412886
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4015n100
Supporting Variantsnssv3729140, nssv3729141, nssv3579981, nssv3579974, nssv3579972, nssv3579975, nssv3579971, nssv3579979, nssv3579976, nssv3579973, nssv3579980, nssv3579978, nssv3579977
Samples
Known GenesANKRD36, ANKRD36B, FAHD2B, LOC100506076, LOC100506123
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013849
Frequency
Sample Size11257
Observed Gain4
Observed Loss9
Observed Complex0
Frequencyn/a


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